Canonical Allele Identifier: CA1279536521

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111929450G= , CM000664.2:g.111929450G=	GRCh38
NC_000002.11:g.112687027G= , CM000664.1:g.112687027G=	GRCh37
NC_000002.10:g.112403498G=	NCBI36
NG_011607.1:g.35837G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.392G= MANE Select	ENSP00000295408.4:p.Trp131=
ENST00000295408.8:c.392G=	ENSP00000295408.4:p.Trp131=
ENST00000409780.5:c.-46-15510G=	ENSP00000387277.1:n.-46-15510G=
ENST00000421804.6:c.392G=	ENSP00000389152.2:p.Trp131=
ENST00000439966.5:c.246+146G=	ENSP00000402129.1:n.246+146G=
ENST00000616902.4:c.-824G=	ENSP00000482824.1:n.-824G=
NM_006343.2:c.392G=	NP_006334.2:p.Trp131=
XM_005263565.3:c.392G=	XP_005263622.1:p.Trp131=
XM_005263568.3:c.392G=	XP_005263625.1:p.Trp131=
XM_011510490.1:c.203G=	XP_011508792.1:p.Trp68=
XM_005263565.4:c.392G=	XP_005263622.1:p.Trp131=
XM_005263568.4:c.392G=	XP_005263625.1:p.Trp131=
XM_011510490.3:c.203G=	XP_011508792.1:p.Trp68=
XM_017003164.1:c.203G=	XP_016858653.1:p.Trp68=
XM_017003165.2:c.-876G=	XP_016858654.1:n.-876G=
NM_006343.3:c.392G= MANE Select	NP_006334.2:p.Trp131=