Canonical Allele Identifier: CA348231160

Gene: MERTK

Linked Data

• MyVariant Identifiers: chr2:g.112754938G>T (hg19) ; chr2:g.111997361G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997361G>T , CM000664.2:g.111997361G>T	GRCh38
NC_000002.11:g.112754938G>T , CM000664.1:g.112754938G>T	GRCh37
NC_000002.10:g.112471409G>T	NCBI36
NG_011607.1:g.103748G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1489G>T MANE Select	ENSP00000295408.4:p.Gly497Cys
ENST00000295408.8:c.1489G>T	ENSP00000295408.4:p.Gly497Cys
ENST00000409780.5:c.961G>T	ENSP00000387277.1:p.Gly321Cys
ENST00000421804.6:c.1489G>T	ENSP00000389152.2:p.Gly497Cys
ENST00000439966.5:c.*962G>T	ENSP00000402129.1:n.*962G>T
ENST00000616902.4:c.458G>T	ENSP00000482824.1:p.Trp153Leu
NM_006343.2:c.1489G>T	NP_006334.2:p.Gly497Cys
XM_005263565.3:c.1489G>T	XP_005263622.1:p.Gly497Cys
XM_005263568.3:c.1489G>T	XP_005263625.1:p.Gly497Cys
XM_011510490.1:c.1300G>T	XP_011508792.1:p.Gly434Cys
XM_011510491.1:c.274G>T	XP_011508793.1:p.Gly92Cys
XM_005263565.4:c.1489G>T	XP_005263622.1:p.Gly497Cys
XM_005263568.4:c.1489G>T	XP_005263625.1:p.Gly497Cys
XM_011510490.3:c.1300G>T	XP_011508792.1:p.Gly434Cys
XM_017003164.1:c.1300G>T	XP_016858653.1:p.Gly434Cys
XM_017003165.2:c.274G>T	XP_016858654.1:p.Gly92Cys
NM_006343.3:c.1489G>T MANE Select	NP_006334.2:p.Gly497Cys