Canonical Allele Identifier: CA1279566551

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997376G= , CM000664.2:g.111997376G=	GRCh38
NC_000002.11:g.112754953G= , CM000664.1:g.112754953G=	GRCh37
NC_000002.10:g.112471424G=	NCBI36
NG_011607.1:g.103763G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1504G= MANE Select	ENSP00000295408.4:p.Val502=
ENST00000295408.8:c.1504G=	ENSP00000295408.4:p.Val502=
ENST00000409780.5:c.976G=	ENSP00000387277.1:p.Val326=
ENST00000421804.6:c.1504G=	ENSP00000389152.2:p.Val502=
ENST00000439966.5:c.*977G=	ENSP00000402129.1:n.*977G=
ENST00000473065.1:n.7G=
ENST00000616902.4:c.473G=	ENSP00000482824.1:p.Cys158=
NM_006343.2:c.1504G=	NP_006334.2:p.Val502=
XM_005263565.3:c.1504G=	XP_005263622.1:p.Val502=
XM_005263568.3:c.1504G=	XP_005263625.1:p.Val502=
XM_011510490.1:c.1315G=	XP_011508792.1:p.Val439=
XM_011510491.1:c.289G=	XP_011508793.1:p.Val97=
XM_005263565.4:c.1504G=	XP_005263622.1:p.Val502=
XM_005263568.4:c.1504G=	XP_005263625.1:p.Val502=
XM_011510490.3:c.1315G=	XP_011508792.1:p.Val439=
XM_017003164.1:c.1315G=	XP_016858653.1:p.Val439=
XM_017003165.2:c.289G=	XP_016858654.1:p.Val97=
NM_006343.3:c.1504G= MANE Select	NP_006334.2:p.Val502=