Canonical Allele Identifier: CA1279566465

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997197C= , CM000664.2:g.111997197C=	GRCh38
NC_000002.11:g.112754774C= , CM000664.1:g.112754774C=	GRCh37
NC_000002.10:g.112471245C=	NCBI36
NG_011607.1:g.103584C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1451-126C= MANE Select	ENSP00000295408.4:n.1451-126C=
ENST00000295408.8:c.1451-126C=	ENSP00000295408.4:n.1451-126C=
ENST00000409780.5:c.923-126C=	ENSP00000387277.1:n.923-126C=
ENST00000421804.6:c.1451-126C=	ENSP00000389152.2:n.1451-126C=
ENST00000439966.5:c.*924-126C=	ENSP00000402129.1:n.*924-126C=
ENST00000616902.4:c.401-52C=	ENSP00000482824.1:n.401-52C=
NM_006343.2:c.1451-126C=	NP_006334.2:n.1451-126C=
XM_005263565.3:c.1451-126C=	XP_005263622.1:n.1451-126C=
XM_005263568.3:c.1451-126C=	XP_005263625.1:n.1451-126C=
XM_011510490.1:c.1262-126C=	XP_011508792.1:n.1262-126C=
XM_011510491.1:c.236-126C=	XP_011508793.1:n.236-126C=
XM_005263565.4:c.1451-126C=	XP_005263622.1:n.1451-126C=
XM_005263568.4:c.1451-126C=	XP_005263625.1:n.1451-126C=
XM_011510490.3:c.1262-126C=	XP_011508792.1:n.1262-126C=
XM_017003164.1:c.1262-126C=	XP_016858653.1:n.1262-126C=
XM_017003165.2:c.236-126C=	XP_016858654.1:n.236-126C=
NM_006343.3:c.1451-126C= MANE Select	NP_006334.2:n.1451-126C=