Canonical Allele Identifier: CA348231346
Gene: MERTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111997396C>T , CM000664.2:g.111997396C>T GRCh38
NC_000002.11:g.112754973C>T , CM000664.1:g.112754973C>T GRCh37
NC_000002.10:g.112471444C>T NCBI36
NG_011607.1:g.103783C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.1524C>T MANE Select ENSP00000295408.4:p.Cys508=
ENST00000295408.8:c.1524C>T ENSP00000295408.4:p.Cys508=
ENST00000409780.5:c.996C>T ENSP00000387277.1:p.Cys332=
ENST00000421804.6:c.1524C>T ENSP00000389152.2:p.Cys508=
ENST00000439966.5:c.*997C>T ENSP00000402129.1:n.*997C>T
ENST00000473065.1:n.27C>T
ENST00000616902.4:c.493C>T ENSP00000482824.1:p.Leu165Phe
NM_006343.2:c.1524C>T NP_006334.2:p.Cys508=
XM_005263565.3:c.1524C>T XP_005263622.1:p.Cys508=
XM_005263568.3:c.1524C>T XP_005263625.1:p.Cys508=
XM_011510490.1:c.1335C>T XP_011508792.1:p.Cys445=
XM_011510491.1:c.309C>T XP_011508793.1:p.Cys103=
XM_005263565.4:c.1524C>T XP_005263622.1:p.Cys508=
XM_005263568.4:c.1524C>T XP_005263625.1:p.Cys508=
XM_011510490.3:c.1335C>T XP_011508792.1:p.Cys445=
XM_017003164.1:c.1335C>T XP_016858653.1:p.Cys445=
XM_017003165.2:c.309C>T XP_016858654.1:p.Cys103=
NM_006343.3:c.1524C>T MANE Select NP_006334.2:p.Cys508=