Canonical Allele Identifier: CA428275224

Gene: MERTK

Linked Data

• gnomAD v4: 2-112008429-A-T
• MyVariant Identifiers: chr2:g.112766006A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112008429A>T , CM000664.2:g.112008429A>T	GRCh38
NC_000002.11:g.112766006A>T , CM000664.1:g.112766006A>T	GRCh37
NC_000002.10:g.112482477A>T	NCBI36
NG_011607.1:g.114816A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1914A>T MANE Select	ENSP00000295408.4:p.Ala638=
ENST00000295408.8:c.1914A>T	ENSP00000295408.4:p.Ala638=
ENST00000409780.5:c.1386A>T	ENSP00000387277.1:p.Ala462=
ENST00000421804.6:c.1914A>T	ENSP00000389152.2:p.Ala638=
ENST00000439966.5:c.*1387A>T	ENSP00000402129.1:n.*1387A>T
ENST00000616902.4:c.879A>T	ENSP00000482824.1:p.Ala293=
NM_006343.2:c.1914A>T	NP_006334.2:p.Ala638=
XM_005263565.3:c.1914A>T	XP_005263622.1:p.Ala638=
XM_005263568.3:c.1914A>T	XP_005263625.1:p.Ala638=
XM_011510490.1:c.1725A>T	XP_011508792.1:p.Ala575=
XM_011510491.1:c.699A>T	XP_011508793.1:p.Ala233=
XM_005263565.4:c.1914A>T	XP_005263622.1:p.Ala638=
XM_005263568.4:c.1914A>T	XP_005263625.1:p.Ala638=
XM_011510490.3:c.1725A>T	XP_011508792.1:p.Ala575=
XM_017003164.1:c.1725A>T	XP_016858653.1:p.Ala575=
XM_017003165.2:c.699A>T	XP_016858654.1:p.Ala233=
NM_006343.3:c.1914A>T MANE Select	NP_006334.2:p.Ala638=