Canonical Allele Identifier: CA1279536506
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111929425_111929427delinsTAC , CM000664.2:g.111929425_111929427delinsTAC GRCh38
NC_000002.11:g.112687002_112687004delinsTAC , CM000664.1:g.112687002_112687004delinsTAC GRCh37
NC_000002.10:g.112403473_112403475delinsTAC NCBI36
NG_011607.1:g.35812_35814delinsTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.367_369delinsTAC MANE Select ENSP00000295408.4:p.Tyr123=
ENST00000295408.8:c.367_369delinsTAC ENSP00000295408.4:p.Tyr123=
ENST00000409780.5:c.-46-15535_-46-15533delinsTAC ENSP00000387277.1:n.-46-15535_-46-15533delinsTAC
ENST00000421804.6:c.367_369delinsTAC ENSP00000389152.2:p.Tyr123=
ENST00000439966.5:c.246+121_246+123delinsTAC ENSP00000402129.1:n.246+121_246+123delinsTAC
ENST00000616902.4:c.-849_-847delinsTAC ENSP00000482824.1:n.-849_-847delinsTAC
NM_006343.2:c.367_369delinsTAC NP_006334.2:p.Tyr123=
XM_005263565.3:c.367_369delinsTAC XP_005263622.1:p.Tyr123=
XM_005263568.3:c.367_369delinsTAC XP_005263625.1:p.Tyr123=
XM_011510490.1:c.178_180delinsTAC XP_011508792.1:p.Tyr60=
XM_005263565.4:c.367_369delinsTAC XP_005263622.1:p.Tyr123=
XM_005263568.4:c.367_369delinsTAC XP_005263625.1:p.Tyr123=
XM_011510490.3:c.178_180delinsTAC XP_011508792.1:p.Tyr60=
XM_017003164.1:c.178_180delinsTAC XP_016858653.1:p.Tyr60=
XM_017003165.2:c.-901_-899delinsTAC XP_016858654.1:n.-901_-899delinsTAC
NM_006343.3:c.367_369delinsTAC MANE Select NP_006334.2:p.Tyr123=