Canonical Allele Identifier: CA428275209

Gene: MERTK

Linked Data

• gnomAD v4: 2-112008399-G-A
• MyVariant Identifiers: chr2:g.112765976G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112008399G>A , CM000664.2:g.112008399G>A	GRCh38
NC_000002.11:g.112765976G>A , CM000664.1:g.112765976G>A	GRCh37
NC_000002.10:g.112482447G>A	NCBI36
NG_011607.1:g.114786G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1884G>A MANE Select	ENSP00000295408.4:p.Gln628=
ENST00000295408.8:c.1884G>A	ENSP00000295408.4:p.Gln628=
ENST00000409780.5:c.1356G>A	ENSP00000387277.1:p.Gln452=
ENST00000421804.6:c.1884G>A	ENSP00000389152.2:p.Gln628=
ENST00000439966.5:c.*1357G>A	ENSP00000402129.1:n.*1357G>A
ENST00000616902.4:c.849G>A	ENSP00000482824.1:p.Gln283=
NM_006343.2:c.1884G>A	NP_006334.2:p.Gln628=
XM_005263565.3:c.1884G>A	XP_005263622.1:p.Gln628=
XM_005263568.3:c.1884G>A	XP_005263625.1:p.Gln628=
XM_011510490.1:c.1695G>A	XP_011508792.1:p.Gln565=
XM_011510491.1:c.669G>A	XP_011508793.1:p.Gln223=
XM_005263565.4:c.1884G>A	XP_005263622.1:p.Gln628=
XM_005263568.4:c.1884G>A	XP_005263625.1:p.Gln628=
XM_011510490.3:c.1695G>A	XP_011508792.1:p.Gln565=
XM_017003164.1:c.1695G>A	XP_016858653.1:p.Gln565=
XM_017003165.2:c.669G>A	XP_016858654.1:p.Gln223=
NM_006343.3:c.1884G>A MANE Select	NP_006334.2:p.Gln628=