Canonical Allele Identifier: CA348229278
Gene: MERTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947541A>G , CM000664.2:g.111947541A>G GRCh38
NC_000002.11:g.112705118A>G , CM000664.1:g.112705118A>G GRCh37
NC_000002.10:g.112421589A>G NCBI36
NG_011607.1:g.53928A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.731A>G MANE Select ENSP00000295408.4:p.Lys244Arg
ENST00000295408.8:c.731A>G ENSP00000295408.4:p.Lys244Arg
ENST00000409780.5:c.203A>G ENSP00000387277.1:p.Lys68Arg
ENST00000421804.6:c.731A>G ENSP00000389152.2:p.Lys244Arg
ENST00000439966.5:c.*204A>G ENSP00000402129.1:n.*204A>G
ENST00000616902.4:c.-485A>G ENSP00000482824.1:n.-485A>G
NM_006343.2:c.731A>G NP_006334.2:p.Lys244Arg
XM_005263565.3:c.731A>G XP_005263622.1:p.Lys244Arg
XM_005263568.3:c.731A>G XP_005263625.1:p.Lys244Arg
XM_011510490.1:c.542A>G XP_011508792.1:p.Lys181Arg
XM_005263565.4:c.731A>G XP_005263622.1:p.Lys244Arg
XM_005263568.4:c.731A>G XP_005263625.1:p.Lys244Arg
XM_011510490.3:c.542A>G XP_011508792.1:p.Lys181Arg
XM_017003164.1:c.542A>G XP_016858653.1:p.Lys181Arg
XM_017003165.2:c.-537A>G XP_016858654.1:n.-537A>G
NM_006343.3:c.731A>G MANE Select NP_006334.2:p.Lys244Arg