Canonical Allele Identifier: CA2660687058
Gene: MERTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947298_111947362del , CM000664.2:g.111947298_111947362del GRCh38
NC_000002.11:g.112704875_112704939del , CM000664.1:g.112704875_112704939del GRCh37
NC_000002.10:g.112421346_112421410del NCBI36
NG_011607.1:g.53685_53749del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.584-96_584-32del MANE Select ENSP00000295408.4:n.584-96_584-32del
ENST00000295408.8:c.584-96_584-32del ENSP00000295408.4:n.584-96_584-32del
ENST00000409780.5:c.56-96_56-32del ENSP00000387277.1:n.56-96_56-32del
ENST00000421804.6:c.584-96_584-32del ENSP00000389152.2:n.584-96_584-32del
ENST00000439966.5:c.*57-96_*57-32del ENSP00000402129.1:n.*57-96_*57-32del
ENST00000616902.4:c.-632-96_-632-32del ENSP00000482824.1:n.-632-96_-632-32del
NM_006343.2:c.584-96_584-32del NP_006334.2:n.584-96_584-32del
XM_005263565.3:c.584-96_584-32del XP_005263622.1:n.584-96_584-32del
XM_005263568.3:c.584-96_584-32del XP_005263625.1:n.584-96_584-32del
XM_011510490.1:c.395-96_395-32del XP_011508792.1:n.395-96_395-32del
XM_005263565.4:c.584-96_584-32del XP_005263622.1:n.584-96_584-32del
XM_005263568.4:c.584-96_584-32del XP_005263625.1:n.584-96_584-32del
XM_011510490.3:c.395-96_395-32del XP_011508792.1:n.395-96_395-32del
XM_017003164.1:c.395-96_395-32del XP_016858653.1:n.395-96_395-32del
XM_017003165.2:c.-684-96_-684-32del XP_016858654.1:n.-684-96_-684-32del
NM_006343.3:c.584-96_584-32del MANE Select NP_006334.2:n.584-96_584-32del