Canonical Allele Identifier: CA2660687127
Gene: MERTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947308_111947309insCAT , CM000664.2:g.111947308_111947309insCAT GRCh38
NC_000002.11:g.112704885_112704886insCAT , CM000664.1:g.112704885_112704886insCAT GRCh37
NC_000002.10:g.112421356_112421357insCAT NCBI36
NG_011607.1:g.53695_53696insCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.584-86_584-85insCAT MANE Select ENSP00000295408.4:n.584-86_584-85insCAT
ENST00000295408.8:c.584-86_584-85insCAT ENSP00000295408.4:n.584-86_584-85insCAT
ENST00000409780.5:c.56-86_56-85insCAT ENSP00000387277.1:n.56-86_56-85insCAT
ENST00000421804.6:c.584-86_584-85insCAT ENSP00000389152.2:n.584-86_584-85insCAT
ENST00000439966.5:c.*57-86_*57-85insCAT ENSP00000402129.1:n.*57-86_*57-85insCAT
ENST00000616902.4:c.-632-86_-632-85insCAT ENSP00000482824.1:n.-632-86_-632-85insCAT
NM_006343.2:c.584-86_584-85insCAT NP_006334.2:n.584-86_584-85insCAT
XM_005263565.3:c.584-86_584-85insCAT XP_005263622.1:n.584-86_584-85insCAT
XM_005263568.3:c.584-86_584-85insCAT XP_005263625.1:n.584-86_584-85insCAT
XM_011510490.1:c.395-86_395-85insCAT XP_011508792.1:n.395-86_395-85insCAT
XM_005263565.4:c.584-86_584-85insCAT XP_005263622.1:n.584-86_584-85insCAT
XM_005263568.4:c.584-86_584-85insCAT XP_005263625.1:n.584-86_584-85insCAT
XM_011510490.3:c.395-86_395-85insCAT XP_011508792.1:n.395-86_395-85insCAT
XM_017003164.1:c.395-86_395-85insCAT XP_016858653.1:n.395-86_395-85insCAT
XM_017003165.2:c.-684-86_-684-85insCAT XP_016858654.1:n.-684-86_-684-85insCAT
NM_006343.3:c.584-86_584-85insCAT MANE Select NP_006334.2:n.584-86_584-85insCAT