Canonical Allele Identifier: CA1279566563

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997397T= , CM000664.2:g.111997397T=	GRCh38
NC_000002.11:g.112754974T= , CM000664.1:g.112754974T=	GRCh37
NC_000002.10:g.112471445T=	NCBI36
NG_011607.1:g.103784T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1525T= MANE Select	ENSP00000295408.4:p.Phe509=
ENST00000295408.8:c.1525T=	ENSP00000295408.4:p.Phe509=
ENST00000409780.5:c.997T=	ENSP00000387277.1:p.Phe333=
ENST00000421804.6:c.1525T=	ENSP00000389152.2:p.Phe509=
ENST00000439966.5:c.*998T=	ENSP00000402129.1:n.*998T=
ENST00000473065.1:n.28T=
ENST00000616902.4:c.494T=	ENSP00000482824.1:p.Leu165=
NM_006343.2:c.1525T=	NP_006334.2:p.Phe509=
XM_005263565.3:c.1525T=	XP_005263622.1:p.Phe509=
XM_005263568.3:c.1525T=	XP_005263625.1:p.Phe509=
XM_011510490.1:c.1336T=	XP_011508792.1:p.Phe446=
XM_011510491.1:c.310T=	XP_011508793.1:p.Phe104=
XM_005263565.4:c.1525T=	XP_005263622.1:p.Phe509=
XM_005263568.4:c.1525T=	XP_005263625.1:p.Phe509=
XM_011510490.3:c.1336T=	XP_011508792.1:p.Phe446=
XM_017003164.1:c.1336T=	XP_016858653.1:p.Phe446=
XM_017003165.2:c.310T=	XP_016858654.1:p.Phe104=
NM_006343.3:c.1525T= MANE Select	NP_006334.2:p.Phe509=