Canonical Allele Identifier: CA1279544296

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947418C= , CM000664.2:g.111947418C=	GRCh38
NC_000002.11:g.112704995C= , CM000664.1:g.112704995C=	GRCh37
NC_000002.10:g.112421466C=	NCBI36
NG_011607.1:g.53805C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.608C= MANE Select	ENSP00000295408.4:p.Pro203=
ENST00000295408.8:c.608C=	ENSP00000295408.4:p.Pro203=
ENST00000409780.5:c.80C=	ENSP00000387277.1:p.Pro27=
ENST00000421804.6:c.608C=	ENSP00000389152.2:p.Pro203=
ENST00000439966.5:c.*81C=	ENSP00000402129.1:n.*81C=
ENST00000616902.4:c.-608C=	ENSP00000482824.1:n.-608C=
NM_006343.2:c.608C=	NP_006334.2:p.Pro203=
XM_005263565.3:c.608C=	XP_005263622.1:p.Pro203=
XM_005263568.3:c.608C=	XP_005263625.1:p.Pro203=
XM_011510490.1:c.419C=	XP_011508792.1:p.Pro140=
XM_005263565.4:c.608C=	XP_005263622.1:p.Pro203=
XM_005263568.4:c.608C=	XP_005263625.1:p.Pro203=
XM_011510490.3:c.419C=	XP_011508792.1:p.Pro140=
XM_017003164.1:c.419C=	XP_016858653.1:p.Pro140=
XM_017003165.2:c.-660C=	XP_016858654.1:n.-660C=
NM_006343.3:c.608C= MANE Select	NP_006334.2:p.Pro203=