Canonical Allele Identifier: CA2765900755

Gene: CPLANE1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37122599_37122600del , CM000667.2:g.37122599_37122600del	GRCh38
NC_000005.9:g.37122701_37122702del , CM000667.1:g.37122701_37122702del	GRCh37
NC_000005.8:g.37158458_37158459del	NCBI36
NG_032772.1:g.131829_131830del
NG_032772.2:g.131829_131830del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651892.2:c.8959-112_8959-111del MANE Select	ENSP00000498265.2:n.8959-112_8959-111del
ENST00000676160.1:n.820-112_820-111del
ENST00000425232.6:c.8797-112_8797-111del	ENSP00000389014.2:n.8797-112_8797-111del
ENST00000508244.5:c.8797-112_8797-111del	ENSP00000421690.1:n.8797-112_8797-111del
ENST00000509849.5:c.5971-112_5971-111del	ENSP00000426337.1:n.5971-112_5971-111del
ENST00000512288.5:n.342-816_342-815del
ENST00000514429.5:c.5995-112_5995-111del	ENSP00000424223.1:n.5995-112_5995-111del
NM_023073.3:c.8797-112_8797-111del	NP_075561.3:n.8797-112_8797-111del
XM_005248345.2:c.8959-112_8959-111del	XP_005248402.1:n.8959-112_8959-111del
XM_005248346.2:c.8956-112_8956-111del	XP_005248403.1:n.8956-112_8956-111del
XM_005248347.2:c.8956-112_8956-111del	XP_005248404.1:n.8956-112_8956-111del
XM_005248349.2:c.8848-112_8848-111del	XP_005248406.1:n.8848-112_8848-111del
XM_005248350.2:c.8830-112_8830-111del	XP_005248407.1:n.8830-112_8830-111del
XM_005248353.3:c.5602-112_5602-111del	XP_005248410.1:n.5602-112_5602-111del
XM_006714489.2:c.8959-112_8959-111del	XP_006714552.1:n.8959-112_8959-111del
XM_006714491.2:c.3532-112_3532-111del	XP_006714554.1:n.3532-112_3532-111del
XM_011514085.1:c.8959-112_8959-111del	XP_011512387.1:n.8959-112_8959-111del
XM_011514086.1:c.8959-112_8959-111del	XP_011512388.1:n.8959-112_8959-111del
XM_011514087.1:c.8905-112_8905-111del	XP_011512389.1:n.8905-112_8905-111del
XM_011514088.1:c.8851-112_8851-111del	XP_011512390.1:n.8851-112_8851-111del
XM_011514089.1:c.8959-112_8959-111del	XP_011512391.1:n.8959-112_8959-111del
XM_011514090.1:c.8641-112_8641-111del	XP_011512392.1:n.8641-112_8641-111del
XM_011514091.1:c.8287-112_8287-111del	XP_011512393.1:n.8287-112_8287-111del
XM_011514092.1:c.8959-112_8959-111del	XP_011512394.1:n.8959-112_8959-111del
XM_011514094.1:c.6184-112_6184-111del	XP_011512396.1:n.6184-112_6184-111del
XR_427661.2:n.9134-112_9134-111del
XR_925644.1:n.9134-112_9134-111del
XM_005248345.4:c.8959-112_8959-111del	XP_005248402.1:n.8959-112_8959-111del
XM_005248346.4:c.8956-112_8956-111del	XP_005248403.1:n.8956-112_8956-111del
XM_005248347.4:c.8956-112_8956-111del	XP_005248404.1:n.8956-112_8956-111del
XM_005248349.4:c.8848-112_8848-111del	XP_005248406.1:n.8848-112_8848-111del
XM_005248350.4:c.8830-112_8830-111del	XP_005248407.1:n.8830-112_8830-111del
XM_006714491.3:c.3532-112_3532-111del	XP_006714554.1:n.3532-112_3532-111del
XM_011514085.3:c.8959-112_8959-111del	XP_011512387.1:n.8959-112_8959-111del
XM_011514086.3:c.8959-112_8959-111del	XP_011512388.1:n.8959-112_8959-111del
XM_011514087.2:c.8905-112_8905-111del	XP_011512389.1:n.8905-112_8905-111del
XM_011514088.2:c.8851-112_8851-111del	XP_011512390.1:n.8851-112_8851-111del
XM_011514089.2:c.8959-112_8959-111del	XP_011512391.1:n.8959-112_8959-111del
XM_011514090.3:c.8641-112_8641-111del	XP_011512392.1:n.8641-112_8641-111del
XM_011514092.2:c.8959-112_8959-111del	XP_011512394.1:n.8959-112_8959-111del
XM_011514094.2:c.6184-112_6184-111del	XP_011512396.1:n.6184-112_6184-111del
XM_017009760.1:c.8770-112_8770-111del	XP_016865249.1:n.8770-112_8770-111del
XM_017009761.2:c.8770-112_8770-111del	XP_016865250.1:n.8770-112_8770-111del
XM_017009763.1:c.7966-112_7966-111del	XP_016865252.1:n.7966-112_7966-111del
XM_017009765.1:c.7771-112_7771-111del	XP_016865254.1:n.7771-112_7771-111del
XM_017009766.1:c.5602-112_5602-111del	XP_016865255.1:n.5602-112_5602-111del
XM_024446183.1:c.8770-112_8770-111del	XP_024301951.1:n.8770-112_8770-111del
XM_024446184.1:c.8641-112_8641-111del	XP_024301952.1:n.8641-112_8641-111del
XM_024446185.1:c.8287-112_8287-111del	XP_024301953.1:n.8287-112_8287-111del
XM_024446186.1:c.7966-112_7966-111del	XP_024301954.1:n.7966-112_7966-111del
XR_925644.2:n.9183-112_9183-111del
NM_001384732.1:c.8959-112_8959-111del MANE Select	NP_001371661.1:n.8959-112_8959-111del
NM_023073.4:c.8797-112_8797-111del	NP_075561.3:n.8797-112_8797-111del