Canonical Allele Identifier: CA1279571262

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112008467G= , CM000664.2:g.112008467G=	GRCh38
NC_000002.11:g.112766044G= , CM000664.1:g.112766044G=	GRCh37
NC_000002.10:g.112482515G=	NCBI36
NG_011607.1:g.114854G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1952G= MANE Select	ENSP00000295408.4:p.Arg651=
ENST00000295408.8:c.1952G=	ENSP00000295408.4:p.Arg651=
ENST00000409780.5:c.1424G=	ENSP00000387277.1:p.Arg475=
ENST00000421804.6:c.1952G=	ENSP00000389152.2:p.Arg651=
ENST00000439966.5:c.*1425G=	ENSP00000402129.1:n.*1425G=
ENST00000616902.4:c.917G=	ENSP00000482824.1:p.Arg306=
NM_006343.2:c.1952G=	NP_006334.2:p.Arg651=
XM_005263565.3:c.1952G=	XP_005263622.1:p.Arg651=
XM_005263568.3:c.1952G=	XP_005263625.1:p.Arg651=
XM_011510490.1:c.1763G=	XP_011508792.1:p.Arg588=
XM_011510491.1:c.737G=	XP_011508793.1:p.Arg246=
XM_005263565.4:c.1952G=	XP_005263622.1:p.Arg651=
XM_005263568.4:c.1952G=	XP_005263625.1:p.Arg651=
XM_011510490.3:c.1763G=	XP_011508792.1:p.Arg588=
XM_017003164.1:c.1763G=	XP_016858653.1:p.Arg588=
XM_017003165.2:c.737G=	XP_016858654.1:p.Arg246=
NM_006343.3:c.1952G= MANE Select	NP_006334.2:p.Arg651=