Canonical Allele Identifier: CA348231359
Gene: MERTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111997399T>A , CM000664.2:g.111997399T>A GRCh38
NC_000002.11:g.112754976T>A , CM000664.1:g.112754976T>A GRCh37
NC_000002.10:g.112471447T>A NCBI36
NG_011607.1:g.103786T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.1527T>A MANE Select ENSP00000295408.4:p.Phe509Leu
ENST00000295408.8:c.1527T>A ENSP00000295408.4:p.Phe509Leu
ENST00000409780.5:c.999T>A ENSP00000387277.1:p.Phe333Leu
ENST00000421804.6:c.1527T>A ENSP00000389152.2:p.Phe509Leu
ENST00000439966.5:c.*1000T>A ENSP00000402129.1:n.*1000T>A
ENST00000473065.1:n.30T>A
ENST00000616902.4:c.496T>A ENSP00000482824.1:p.Leu166Met
NM_006343.2:c.1527T>A NP_006334.2:p.Phe509Leu
XM_005263565.3:c.1527T>A XP_005263622.1:p.Phe509Leu
XM_005263568.3:c.1527T>A XP_005263625.1:p.Phe509Leu
XM_011510490.1:c.1338T>A XP_011508792.1:p.Phe446Leu
XM_011510491.1:c.312T>A XP_011508793.1:p.Phe104Leu
XM_005263565.4:c.1527T>A XP_005263622.1:p.Phe509Leu
XM_005263568.4:c.1527T>A XP_005263625.1:p.Phe509Leu
XM_011510490.3:c.1338T>A XP_011508792.1:p.Phe446Leu
XM_017003164.1:c.1338T>A XP_016858653.1:p.Phe446Leu
XM_017003165.2:c.312T>A XP_016858654.1:p.Phe104Leu
NM_006343.3:c.1527T>A MANE Select NP_006334.2:p.Phe509Leu