Canonical Allele Identifier: CA1279544311
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947468G= , CM000664.2:g.111947468G= GRCh38
NC_000002.11:g.112705045G= , CM000664.1:g.112705045G= GRCh37
NC_000002.10:g.112421516G= NCBI36
NG_011607.1:g.53855G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.658G= MANE Select ENSP00000295408.4:p.Ala220=
ENST00000295408.8:c.658G= ENSP00000295408.4:p.Ala220=
ENST00000409780.5:c.130G= ENSP00000387277.1:p.Ala44=
ENST00000421804.6:c.658G= ENSP00000389152.2:p.Ala220=
ENST00000439966.5:c.*131G= ENSP00000402129.1:n.*131G=
ENST00000616902.4:c.-558G= ENSP00000482824.1:n.-558G=
NM_006343.2:c.658G= NP_006334.2:p.Ala220=
XM_005263565.3:c.658G= XP_005263622.1:p.Ala220=
XM_005263568.3:c.658G= XP_005263625.1:p.Ala220=
XM_011510490.1:c.469G= XP_011508792.1:p.Ala157=
XM_005263565.4:c.658G= XP_005263622.1:p.Ala220=
XM_005263568.4:c.658G= XP_005263625.1:p.Ala220=
XM_011510490.3:c.469G= XP_011508792.1:p.Ala157=
XM_017003164.1:c.469G= XP_016858653.1:p.Ala157=
XM_017003165.2:c.-610G= XP_016858654.1:n.-610G=
NM_006343.3:c.658G= MANE Select NP_006334.2:p.Ala220=