Canonical Allele Identifier: CA2660687061
Gene: MERTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947297_111947298insACA , CM000664.2:g.111947297_111947298insACA GRCh38
NC_000002.11:g.112704874_112704875insACA , CM000664.1:g.112704874_112704875insACA GRCh37
NC_000002.10:g.112421345_112421346insACA NCBI36
NG_011607.1:g.53684_53685insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.584-97_584-96insACA MANE Select ENSP00000295408.4:n.584-97_584-96insACA
ENST00000295408.8:c.584-97_584-96insACA ENSP00000295408.4:n.584-97_584-96insACA
ENST00000409780.5:c.56-97_56-96insACA ENSP00000387277.1:n.56-97_56-96insACA
ENST00000421804.6:c.584-97_584-96insACA ENSP00000389152.2:n.584-97_584-96insACA
ENST00000439966.5:c.*57-97_*57-96insACA ENSP00000402129.1:n.*57-97_*57-96insACA
ENST00000616902.4:c.-632-97_-632-96insACA ENSP00000482824.1:n.-632-97_-632-96insACA
NM_006343.2:c.584-97_584-96insACA NP_006334.2:n.584-97_584-96insACA
XM_005263565.3:c.584-97_584-96insACA XP_005263622.1:n.584-97_584-96insACA
XM_005263568.3:c.584-97_584-96insACA XP_005263625.1:n.584-97_584-96insACA
XM_011510490.1:c.395-97_395-96insACA XP_011508792.1:n.395-97_395-96insACA
XM_005263565.4:c.584-97_584-96insACA XP_005263622.1:n.584-97_584-96insACA
XM_005263568.4:c.584-97_584-96insACA XP_005263625.1:n.584-97_584-96insACA
XM_011510490.3:c.395-97_395-96insACA XP_011508792.1:n.395-97_395-96insACA
XM_017003164.1:c.395-97_395-96insACA XP_016858653.1:n.395-97_395-96insACA
XM_017003165.2:c.-684-97_-684-96insACA XP_016858654.1:n.-684-97_-684-96insACA
NM_006343.3:c.584-97_584-96insACA MANE Select NP_006334.2:n.584-97_584-96insACA