Canonical Allele Identifier: CA1279566544
Gene: MERTK HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.1489G= MANE Select ENSP00000295408.4:p.Gly497=
ENST00000295408.8:c.1489G= ENSP00000295408.4:p.Gly497=
ENST00000409780.5:c.961G= ENSP00000387277.1:p.Gly321=
ENST00000421804.6:c.1489G= ENSP00000389152.2:p.Gly497=
ENST00000439966.5:c.*962G= ENSP00000402129.1:n.*962G=
ENST00000616902.4:c.458G= ENSP00000482824.1:p.Trp153=
NM_006343.2:c.1489G= NP_006334.2:p.Gly497=
XM_005263565.3:c.1489G= XP_005263622.1:p.Gly497=
XM_005263568.3:c.1489G= XP_005263625.1:p.Gly497=
XM_011510490.1:c.1300G= XP_011508792.1:p.Gly434=
XM_011510491.1:c.274G= XP_011508793.1:p.Gly92=
XM_005263565.4:c.1489G= XP_005263622.1:p.Gly497=
XM_005263568.4:c.1489G= XP_005263625.1:p.Gly497=
XM_011510490.3:c.1300G= XP_011508792.1:p.Gly434=
XM_017003164.1:c.1300G= XP_016858653.1:p.Gly434=
XM_017003165.2:c.274G= XP_016858654.1:p.Gly92=
NM_006343.3:c.1489G= MANE Select NP_006334.2:p.Gly497=