Canonical Allele Identifier: CA2739770861

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997204T>A , CM000664.2:g.111997204T>A	GRCh38
NC_000002.11:g.112754781T>A , CM000664.1:g.112754781T>A	GRCh37
NC_000002.10:g.112471252T>A	NCBI36
NG_011607.1:g.103591T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1451-119T>A MANE Select	ENSP00000295408.4:n.1451-119T>A
ENST00000295408.8:c.1451-119T>A	ENSP00000295408.4:n.1451-119T>A
ENST00000409780.5:c.923-119T>A	ENSP00000387277.1:n.923-119T>A
ENST00000421804.6:c.1451-119T>A	ENSP00000389152.2:n.1451-119T>A
ENST00000439966.5:c.*924-119T>A	ENSP00000402129.1:n.*924-119T>A
ENST00000616902.4:c.401-45T>A	ENSP00000482824.1:n.401-45T>A
NM_006343.2:c.1451-119T>A	NP_006334.2:n.1451-119T>A
XM_005263565.3:c.1451-119T>A	XP_005263622.1:n.1451-119T>A
XM_005263568.3:c.1451-119T>A	XP_005263625.1:n.1451-119T>A
XM_011510490.1:c.1262-119T>A	XP_011508792.1:n.1262-119T>A
XM_011510491.1:c.236-119T>A	XP_011508793.1:n.236-119T>A
XM_005263565.4:c.1451-119T>A	XP_005263622.1:n.1451-119T>A
XM_005263568.4:c.1451-119T>A	XP_005263625.1:n.1451-119T>A
XM_011510490.3:c.1262-119T>A	XP_011508792.1:n.1262-119T>A
XM_017003164.1:c.1262-119T>A	XP_016858653.1:n.1262-119T>A
XM_017003165.2:c.236-119T>A	XP_016858654.1:n.236-119T>A
NM_006343.3:c.1451-119T>A MANE Select	NP_006334.2:n.1451-119T>A