Canonical Allele Identifier: CA2765900815

Gene: CPLANE1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37122646_37122647insCTT , CM000667.2:g.37122646_37122647insCTT	GRCh38
NC_000005.9:g.37122748_37122749insCTT , CM000667.1:g.37122748_37122749insCTT	GRCh37
NC_000005.8:g.37158505_37158506insCTT	NCBI36
NG_032772.1:g.131782_131783insAAG
NG_032772.2:g.131782_131783insAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651892.2:c.8959-159_8959-158insAAG MANE Select	ENSP00000498265.2:n.8959-159_8959-158insAAG
ENST00000676160.1:n.820-159_820-158insAAG
ENST00000425232.6:c.8797-159_8797-158insAAG	ENSP00000389014.2:n.8797-159_8797-158insAAG
ENST00000508244.5:c.8797-159_8797-158insAAG	ENSP00000421690.1:n.8797-159_8797-158insAAG
ENST00000509849.5:c.5971-159_5971-158insAAG	ENSP00000426337.1:n.5971-159_5971-158insAAG
ENST00000512288.5:n.342-863_342-862insAAG
ENST00000514429.5:c.5995-159_5995-158insAAG	ENSP00000424223.1:n.5995-159_5995-158insAAG
NM_023073.3:c.8797-159_8797-158insAAG	NP_075561.3:n.8797-159_8797-158insAAG
XM_005248345.2:c.8959-159_8959-158insAAG	XP_005248402.1:n.8959-159_8959-158insAAG
XM_005248346.2:c.8956-159_8956-158insAAG	XP_005248403.1:n.8956-159_8956-158insAAG
XM_005248347.2:c.8956-159_8956-158insAAG	XP_005248404.1:n.8956-159_8956-158insAAG
XM_005248349.2:c.8848-159_8848-158insAAG	XP_005248406.1:n.8848-159_8848-158insAAG
XM_005248350.2:c.8830-159_8830-158insAAG	XP_005248407.1:n.8830-159_8830-158insAAG
XM_005248353.3:c.5602-159_5602-158insAAG	XP_005248410.1:n.5602-159_5602-158insAAG
XM_006714489.2:c.8959-159_8959-158insAAG	XP_006714552.1:n.8959-159_8959-158insAAG
XM_006714491.2:c.3532-159_3532-158insAAG	XP_006714554.1:n.3532-159_3532-158insAAG
XM_011514085.1:c.8959-159_8959-158insAAG	XP_011512387.1:n.8959-159_8959-158insAAG
XM_011514086.1:c.8959-159_8959-158insAAG	XP_011512388.1:n.8959-159_8959-158insAAG
XM_011514087.1:c.8905-159_8905-158insAAG	XP_011512389.1:n.8905-159_8905-158insAAG
XM_011514088.1:c.8851-159_8851-158insAAG	XP_011512390.1:n.8851-159_8851-158insAAG
XM_011514089.1:c.8959-159_8959-158insAAG	XP_011512391.1:n.8959-159_8959-158insAAG
XM_011514090.1:c.8641-159_8641-158insAAG	XP_011512392.1:n.8641-159_8641-158insAAG
XM_011514091.1:c.8287-159_8287-158insAAG	XP_011512393.1:n.8287-159_8287-158insAAG
XM_011514092.1:c.8959-159_8959-158insAAG	XP_011512394.1:n.8959-159_8959-158insAAG
XM_011514094.1:c.6184-159_6184-158insAAG	XP_011512396.1:n.6184-159_6184-158insAAG
XR_427661.2:n.9134-159_9134-158insAAG
XR_925644.1:n.9134-159_9134-158insAAG
XM_005248345.4:c.8959-159_8959-158insAAG	XP_005248402.1:n.8959-159_8959-158insAAG
XM_005248346.4:c.8956-159_8956-158insAAG	XP_005248403.1:n.8956-159_8956-158insAAG
XM_005248347.4:c.8956-159_8956-158insAAG	XP_005248404.1:n.8956-159_8956-158insAAG
XM_005248349.4:c.8848-159_8848-158insAAG	XP_005248406.1:n.8848-159_8848-158insAAG
XM_005248350.4:c.8830-159_8830-158insAAG	XP_005248407.1:n.8830-159_8830-158insAAG
XM_006714491.3:c.3532-159_3532-158insAAG	XP_006714554.1:n.3532-159_3532-158insAAG
XM_011514085.3:c.8959-159_8959-158insAAG	XP_011512387.1:n.8959-159_8959-158insAAG
XM_011514086.3:c.8959-159_8959-158insAAG	XP_011512388.1:n.8959-159_8959-158insAAG
XM_011514087.2:c.8905-159_8905-158insAAG	XP_011512389.1:n.8905-159_8905-158insAAG
XM_011514088.2:c.8851-159_8851-158insAAG	XP_011512390.1:n.8851-159_8851-158insAAG
XM_011514089.2:c.8959-159_8959-158insAAG	XP_011512391.1:n.8959-159_8959-158insAAG
XM_011514090.3:c.8641-159_8641-158insAAG	XP_011512392.1:n.8641-159_8641-158insAAG
XM_011514092.2:c.8959-159_8959-158insAAG	XP_011512394.1:n.8959-159_8959-158insAAG
XM_011514094.2:c.6184-159_6184-158insAAG	XP_011512396.1:n.6184-159_6184-158insAAG
XM_017009760.1:c.8770-159_8770-158insAAG	XP_016865249.1:n.8770-159_8770-158insAAG
XM_017009761.2:c.8770-159_8770-158insAAG	XP_016865250.1:n.8770-159_8770-158insAAG
XM_017009763.1:c.7966-159_7966-158insAAG	XP_016865252.1:n.7966-159_7966-158insAAG
XM_017009765.1:c.7771-159_7771-158insAAG	XP_016865254.1:n.7771-159_7771-158insAAG
XM_017009766.1:c.5602-159_5602-158insAAG	XP_016865255.1:n.5602-159_5602-158insAAG
XM_024446183.1:c.8770-159_8770-158insAAG	XP_024301951.1:n.8770-159_8770-158insAAG
XM_024446184.1:c.8641-159_8641-158insAAG	XP_024301952.1:n.8641-159_8641-158insAAG
XM_024446185.1:c.8287-159_8287-158insAAG	XP_024301953.1:n.8287-159_8287-158insAAG
XM_024446186.1:c.7966-159_7966-158insAAG	XP_024301954.1:n.7966-159_7966-158insAAG
XR_925644.2:n.9183-159_9183-158insAAG
NM_001384732.1:c.8959-159_8959-158insAAG MANE Select	NP_001371661.1:n.8959-159_8959-158insAAG
NM_023073.4:c.8797-159_8797-158insAAG	NP_075561.3:n.8797-159_8797-158insAAG