Canonical Allele Identifier: CA1279544318

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947482T= , CM000664.2:g.111947482T=	GRCh38
NC_000002.11:g.112705059T= , CM000664.1:g.112705059T=	GRCh37
NC_000002.10:g.112421530T=	NCBI36
NG_011607.1:g.53869T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.672T= MANE Select	ENSP00000295408.4:p.Pro224=
ENST00000295408.8:c.672T=	ENSP00000295408.4:p.Pro224=
ENST00000409780.5:c.144T=	ENSP00000387277.1:p.Pro48=
ENST00000421804.6:c.672T=	ENSP00000389152.2:p.Pro224=
ENST00000439966.5:c.*145T=	ENSP00000402129.1:n.*145T=
ENST00000616902.4:c.-544T=	ENSP00000482824.1:n.-544T=
NM_006343.2:c.672T=	NP_006334.2:p.Pro224=
XM_005263565.3:c.672T=	XP_005263622.1:p.Pro224=
XM_005263568.3:c.672T=	XP_005263625.1:p.Pro224=
XM_011510490.1:c.483T=	XP_011508792.1:p.Pro161=
XM_005263565.4:c.672T=	XP_005263622.1:p.Pro224=
XM_005263568.4:c.672T=	XP_005263625.1:p.Pro224=
XM_011510490.3:c.483T=	XP_011508792.1:p.Pro161=
XM_017003164.1:c.483T=	XP_016858653.1:p.Pro161=
XM_017003165.2:c.-596T=	XP_016858654.1:n.-596T=
NM_006343.3:c.672T= MANE Select	NP_006334.2:p.Pro224=