Canonical Allele Identifier: CA1279566553
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111997381C= , CM000664.2:g.111997381C= GRCh38
NC_000002.11:g.112754958C= , CM000664.1:g.112754958C= GRCh37
NC_000002.10:g.112471429C= NCBI36
NG_011607.1:g.103768C=

Transcript Alleles

HGVS Amino-acid change
ENST00000295408.9:c.1509C= MANE Select ENSP00000295408.4:p.Leu503=
ENST00000295408.8:c.1509C= ENSP00000295408.4:p.Leu503=
ENST00000409780.5:c.981C= ENSP00000387277.1:p.Leu327=
ENST00000421804.6:c.1509C= ENSP00000389152.2:p.Leu503=
ENST00000439966.5:c.*982C= ENSP00000402129.1:n.*982C=
ENST00000473065.1:n.12C=
ENST00000616902.4:c.478C= ENSP00000482824.1:p.His160=
NM_006343.2:c.1509C= NP_006334.2:p.Leu503=
XM_005263565.3:c.1509C= XP_005263622.1:p.Leu503=
XM_005263568.3:c.1509C= XP_005263625.1:p.Leu503=
XM_011510490.1:c.1320C= XP_011508792.1:p.Leu440=
XM_011510491.1:c.294C= XP_011508793.1:p.Leu98=
XM_005263565.4:c.1509C= XP_005263622.1:p.Leu503=
XM_005263568.4:c.1509C= XP_005263625.1:p.Leu503=
XM_011510490.3:c.1320C= XP_011508792.1:p.Leu440=
XM_017003164.1:c.1320C= XP_016858653.1:p.Leu440=
XM_017003165.2:c.294C= XP_016858654.1:p.Leu98=
NM_006343.3:c.1509C= MANE Select NP_006334.2:p.Leu503=