Canonical Allele Identifier: CA348226869
Gene: MERTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111929513A>G , CM000664.2:g.111929513A>G GRCh38
NC_000002.11:g.112687090A>G , CM000664.1:g.112687090A>G GRCh37
NC_000002.10:g.112403561A>G NCBI36
NG_011607.1:g.35900A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.455A>G MANE Select ENSP00000295408.4:p.Glu152Gly
ENST00000295408.8:c.455A>G ENSP00000295408.4:p.Glu152Gly
ENST00000409780.5:c.-46-15447A>G ENSP00000387277.1:n.-46-15447A>G
ENST00000421804.6:c.455A>G ENSP00000389152.2:p.Glu152Gly
ENST00000439966.5:c.246+209A>G ENSP00000402129.1:n.246+209A>G
ENST00000616902.4:c.-761A>G ENSP00000482824.1:n.-761A>G
NM_006343.2:c.455A>G NP_006334.2:p.Glu152Gly
XM_005263565.3:c.455A>G XP_005263622.1:p.Glu152Gly
XM_005263568.3:c.455A>G XP_005263625.1:p.Glu152Gly
XM_011510490.1:c.266A>G XP_011508792.1:p.Glu89Gly
XM_005263565.4:c.455A>G XP_005263622.1:p.Glu152Gly
XM_005263568.4:c.455A>G XP_005263625.1:p.Glu152Gly
XM_011510490.3:c.266A>G XP_011508792.1:p.Glu89Gly
XM_017003164.1:c.266A>G XP_016858653.1:p.Glu89Gly
XM_017003165.2:c.-813A>G XP_016858654.1:n.-813A>G
NM_006343.3:c.455A>G MANE Select NP_006334.2:p.Glu152Gly