Canonical Allele Identifier: CA755213750
Gene: MERTK HGNC NCBI

Linked Data

dbSNP Id: rs1420843375

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947349_111947350del , CM000664.2:g.111947349_111947350del GRCh38
NC_000002.11:g.112704926_112704927del , CM000664.1:g.112704926_112704927del GRCh37
NC_000002.10:g.112421397_112421398del NCBI36
NG_011607.1:g.53736_53737del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.584-45_584-44del MANE Select ENSP00000295408.4:n.584-45_584-44del
ENST00000295408.8:c.584-45_584-44del ENSP00000295408.4:n.584-45_584-44del
ENST00000409780.5:c.56-45_56-44del ENSP00000387277.1:n.56-45_56-44del
ENST00000421804.6:c.584-45_584-44del ENSP00000389152.2:n.584-45_584-44del
ENST00000439966.5:c.*57-45_*57-44del ENSP00000402129.1:n.*57-45_*57-44del
ENST00000616902.4:c.-632-45_-632-44del ENSP00000482824.1:n.-632-45_-632-44del
NM_006343.2:c.584-45_584-44del NP_006334.2:n.584-45_584-44del
XM_005263565.3:c.584-45_584-44del XP_005263622.1:n.584-45_584-44del
XM_005263568.3:c.584-45_584-44del XP_005263625.1:n.584-45_584-44del
XM_011510490.1:c.395-45_395-44del XP_011508792.1:n.395-45_395-44del
XM_005263565.4:c.584-45_584-44del XP_005263622.1:n.584-45_584-44del
XM_005263568.4:c.584-45_584-44del XP_005263625.1:n.584-45_584-44del
XM_011510490.3:c.395-45_395-44del XP_011508792.1:n.395-45_395-44del
XM_017003164.1:c.395-45_395-44del XP_016858653.1:n.395-45_395-44del
XM_017003165.2:c.-684-45_-684-44del XP_016858654.1:n.-684-45_-684-44del
NM_006343.3:c.584-45_584-44del MANE Select NP_006334.2:n.584-45_584-44del