Canonical Allele Identifier: CA428270316

Gene: MERTK

Linked Data

• dbSNP Id: rs1573592011
• MyVariant Identifiers: chr2:g.112705059T>A (hg19)

Genomic Alleles

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

Transcript Alleles

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