Canonical Allele Identifier: CA1279544340

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947527C= , CM000664.2:g.111947527C=	GRCh38
NC_000002.11:g.112705104C= , CM000664.1:g.112705104C=	GRCh37
NC_000002.10:g.112421575C=	NCBI36
NG_011607.1:g.53914C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.717C= MANE Select	ENSP00000295408.4:p.Asn239=
ENST00000295408.8:c.717C=	ENSP00000295408.4:p.Asn239=
ENST00000409780.5:c.189C=	ENSP00000387277.1:p.Asn63=
ENST00000421804.6:c.717C=	ENSP00000389152.2:p.Asn239=
ENST00000439966.5:c.*190C=	ENSP00000402129.1:n.*190C=
ENST00000616902.4:c.-499C=	ENSP00000482824.1:n.-499C=
NM_006343.2:c.717C=	NP_006334.2:p.Asn239=
XM_005263565.3:c.717C=	XP_005263622.1:p.Asn239=
XM_005263568.3:c.717C=	XP_005263625.1:p.Asn239=
XM_011510490.1:c.528C=	XP_011508792.1:p.Asn176=
XM_005263565.4:c.717C=	XP_005263622.1:p.Asn239=
XM_005263568.4:c.717C=	XP_005263625.1:p.Asn239=
XM_011510490.3:c.528C=	XP_011508792.1:p.Asn176=
XM_017003164.1:c.528C=	XP_016858653.1:p.Asn176=
XM_017003165.2:c.-551C=	XP_016858654.1:n.-551C=
NM_006343.3:c.717C= MANE Select	NP_006334.2:p.Asn239=