Canonical Allele Identifier: CA53574428

Gene: MERTK

Linked Data

• dbSNP Id: rs1046528455
• gnomAD v2: 2-112754969-G-A
• gnomAD v4: 2-111997392-G-A
• MyVariant Identifiers: chr2:g.112754969G>A (hg19) ; chr2:g.111997392G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997392G>A , CM000664.2:g.111997392G>A	GRCh38
NC_000002.11:g.112754969G>A , CM000664.1:g.112754969G>A	GRCh37
NC_000002.10:g.112471440G>A	NCBI36
NG_011607.1:g.103779G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1520G>A MANE Select	ENSP00000295408.4:p.Gly507Asp
ENST00000295408.8:c.1520G>A	ENSP00000295408.4:p.Gly507Asp
ENST00000409780.5:c.992G>A	ENSP00000387277.1:p.Gly331Asp
ENST00000421804.6:c.1520G>A	ENSP00000389152.2:p.Gly507Asp
ENST00000439966.5:c.*993G>A	ENSP00000402129.1:n.*993G>A
ENST00000473065.1:n.23G>A
ENST00000616902.4:c.489G>A	ENSP00000482824.1:p.Trp163Ter
NM_006343.2:c.1520G>A	NP_006334.2:p.Gly507Asp
XM_005263565.3:c.1520G>A	XP_005263622.1:p.Gly507Asp
XM_005263568.3:c.1520G>A	XP_005263625.1:p.Gly507Asp
XM_011510490.1:c.1331G>A	XP_011508792.1:p.Gly444Asp
XM_011510491.1:c.305G>A	XP_011508793.1:p.Gly102Asp
XM_005263565.4:c.1520G>A	XP_005263622.1:p.Gly507Asp
XM_005263568.4:c.1520G>A	XP_005263625.1:p.Gly507Asp
XM_011510490.3:c.1331G>A	XP_011508792.1:p.Gly444Asp
XM_017003164.1:c.1331G>A	XP_016858653.1:p.Gly444Asp
XM_017003165.2:c.305G>A	XP_016858654.1:p.Gly102Asp
NM_006343.3:c.1520G>A MANE Select	NP_006334.2:p.Gly507Asp