Canonical Allele Identifier: CA1831831

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112022343A>G , CM000664.2:g.112022343A>G	GRCh38
NC_000002.11:g.112779920A>G , CM000664.1:g.112779920A>G	GRCh37
NC_000002.10:g.112496391A>G	NCBI36
NG_011607.1:g.128730A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006343.3:c.2435A>G MANE Select	NP_006334.2:p.Tyr812Cys
ENST00000295408.9:c.2435A>G MANE Select	ENSP00000295408.4:p.Tyr812Cys
NM_006343.2:c.2435A>G	NP_006334.2:p.Tyr812Cys
ENST00000295408.8:c.2435A>G	ENSP00000295408.4:p.Tyr812Cys
ENST00000409780.5:c.1907A>G	ENSP00000387277.1:p.Tyr636Cys
ENST00000421804.6:c.2435A>G	ENSP00000389152.2:p.Tyr812Cys
ENST00000439966.5:c.*1908A>G	ENSP00000402129.1:n.*1908A>G
ENST00000449344.2:c.407A>G	ENSP00000412660.2:p.Tyr136Cys
ENST00000616902.4:c.1391A>G	ENSP00000482824.1:p.Tyr464Cys
XM_005263565.3:c.2435A>G	XP_005263622.1:p.Tyr812Cys
XM_005263565.4:c.2435A>G	XP_005263622.1:p.Tyr812Cys
XM_011510490.1:c.2246A>G	XP_011508792.1:p.Tyr749Cys
XM_011510490.3:c.2246A>G	XP_011508792.1:p.Tyr749Cys
XM_011510491.1:c.1220A>G	XP_011508793.1:p.Tyr407Cys
XM_017003164.1:c.2246A>G	XP_016858653.1:p.Tyr749Cys
XM_017003165.2:c.1220A>G	XP_016858654.1:p.Tyr407Cys