Canonical Allele Identifier: CA1279566533

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997337G= , CM000664.2:g.111997337G=	GRCh38
NC_000002.11:g.112754914G= , CM000664.1:g.112754914G=	GRCh37
NC_000002.10:g.112471385G=	NCBI36
NG_011607.1:g.103724G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1465G= MANE Select	ENSP00000295408.4:p.Ala489=
ENST00000295408.8:c.1465G=	ENSP00000295408.4:p.Ala489=
ENST00000409780.5:c.937G=	ENSP00000387277.1:p.Ala313=
ENST00000421804.6:c.1465G=	ENSP00000389152.2:p.Ala489=
ENST00000439966.5:c.*938G=	ENSP00000402129.1:n.*938G=
ENST00000616902.4:c.434G=	ENSP00000482824.1:p.Cys145=
NM_006343.2:c.1465G=	NP_006334.2:p.Ala489=
XM_005263565.3:c.1465G=	XP_005263622.1:p.Ala489=
XM_005263568.3:c.1465G=	XP_005263625.1:p.Ala489=
XM_011510490.1:c.1276G=	XP_011508792.1:p.Ala426=
XM_011510491.1:c.250G=	XP_011508793.1:p.Ala84=
XM_005263565.4:c.1465G=	XP_005263622.1:p.Ala489=
XM_005263568.4:c.1465G=	XP_005263625.1:p.Ala489=
XM_011510490.3:c.1276G=	XP_011508792.1:p.Ala426=
XM_017003164.1:c.1276G=	XP_016858653.1:p.Ala426=
XM_017003165.2:c.250G=	XP_016858654.1:p.Ala84=
NM_006343.3:c.1465G= MANE Select	NP_006334.2:p.Ala489=