Canonical Allele Identifier: CA359473820

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37153922A>T (hg19) ; chr5:g.37153820A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37153820A>T , CM000667.2:g.37153820A>T	GRCh38
NC_000005.9:g.37153922A>T , CM000667.1:g.37153922A>T	GRCh37
NC_000005.8:g.37189679A>T	NCBI36
NG_032772.1:g.100609T>A
NG_032772.2:g.100609T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1292T>A
ENST00000651892.2:c.8293T>A MANE Select	ENSP00000498265.2:p.Leu2765Met
ENST00000425232.6:c.8131T>A	ENSP00000389014.2:p.Leu2711Met
ENST00000508244.5:c.8131T>A	ENSP00000421690.1:p.Leu2711Met
ENST00000508405.1:n.25T>A
ENST00000509849.5:c.5305T>A	ENSP00000426337.1:p.Leu1769Met
ENST00000509957.5:n.535T>A
ENST00000511824.2:c.1407T>A
ENST00000514429.5:c.5329T>A	ENSP00000424223.1:p.Leu1777Met
NM_023073.3:c.8131T>A	NP_075561.3:p.Leu2711Met
XM_005248345.2:c.8293T>A	XP_005248402.1:p.Leu2765Met
XM_005248346.2:c.8290T>A	XP_005248403.1:p.Leu2764Met
XM_005248347.2:c.8290T>A	XP_005248404.1:p.Leu2764Met
XM_005248349.2:c.8182T>A	XP_005248406.1:p.Leu2728Met
XM_005248350.2:c.8164T>A	XP_005248407.1:p.Leu2722Met
XM_005248353.3:c.4936T>A	XP_005248410.1:p.Leu1646Met
XM_006714489.2:c.8293T>A	XP_006714552.1:p.Leu2765Met
XM_006714491.2:c.2866T>A	XP_006714554.1:p.Leu956Met
XM_011514085.1:c.8293T>A	XP_011512387.1:p.Leu2765Met
XM_011514086.1:c.8293T>A	XP_011512388.1:p.Leu2765Met
XM_011514087.1:c.8239T>A	XP_011512389.1:p.Leu2747Met
XM_011514088.1:c.8185T>A	XP_011512390.1:p.Leu2729Met
XM_011514089.1:c.8293T>A	XP_011512391.1:p.Leu2765Met
XM_011514090.1:c.7975T>A	XP_011512392.1:p.Leu2659Met
XM_011514091.1:c.7621T>A	XP_011512393.1:p.Leu2541Met
XM_011514092.1:c.8293T>A	XP_011512394.1:p.Leu2765Met
XM_011514094.1:c.5518T>A	XP_011512396.1:p.Leu1840Met
XR_427661.2:n.8468T>A
XR_925644.1:n.8468T>A
XM_005248345.4:c.8293T>A	XP_005248402.1:p.Leu2765Met
XM_005248346.4:c.8290T>A	XP_005248403.1:p.Leu2764Met
XM_005248347.4:c.8290T>A	XP_005248404.1:p.Leu2764Met
XM_005248349.4:c.8182T>A	XP_005248406.1:p.Leu2728Met
XM_005248350.4:c.8164T>A	XP_005248407.1:p.Leu2722Met
XM_006714491.3:c.2866T>A	XP_006714554.1:p.Leu956Met
XM_011514085.3:c.8293T>A	XP_011512387.1:p.Leu2765Met
XM_011514086.3:c.8293T>A	XP_011512388.1:p.Leu2765Met
XM_011514087.2:c.8239T>A	XP_011512389.1:p.Leu2747Met
XM_011514088.2:c.8185T>A	XP_011512390.1:p.Leu2729Met
XM_011514089.2:c.8293T>A	XP_011512391.1:p.Leu2765Met
XM_011514090.3:c.7975T>A	XP_011512392.1:p.Leu2659Met
XM_011514092.2:c.8293T>A	XP_011512394.1:p.Leu2765Met
XM_011514094.2:c.5518T>A	XP_011512396.1:p.Leu1840Met
XM_017009760.1:c.8104T>A	XP_016865249.1:p.Leu2702Met
XM_017009761.2:c.8104T>A	XP_016865250.1:p.Leu2702Met
XM_017009763.1:c.7300T>A	XP_016865252.1:p.Leu2434Met
XM_017009765.1:c.7105T>A	XP_016865254.1:p.Leu2369Met
XM_017009766.1:c.4936T>A	XP_016865255.1:p.Leu1646Met
XM_024446183.1:c.8104T>A	XP_024301951.1:p.Leu2702Met
XM_024446184.1:c.7975T>A	XP_024301952.1:p.Leu2659Met
XM_024446185.1:c.7621T>A	XP_024301953.1:p.Leu2541Met
XM_024446186.1:c.7300T>A	XP_024301954.1:p.Leu2434Met
XR_001742208.1:n.8462T>A
XR_002956171.1:n.8408T>A
XR_925644.2:n.8517T>A
NM_001384732.1:c.8293T>A MANE Select	NP_001371661.1:p.Leu2765Met
NM_023073.4:c.8131T>A	NP_075561.3:p.Leu2711Met