Canonical Allele Identifier: CA2740595971
Gene: ANXA10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165406_168165407insAAAAAAAAAAAAAAAAAAAAAA , CM000666.2:g.168165406_168165407insAAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000004.11:g.169086557_169086558insAAAAAAAAAAAAAAAAAAAAAA , CM000666.1:g.169086557_169086558insAAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000004.10:g.169323132_169323133insAAAAAAAAAAAAAAAAAAAAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+80_480+81insAAAAAAAAAAAAAAAAAAAAAA MANE Select ENSP00000352248.3:n.480+80_480+81insAAAAAAAAAAAAAAAAAAAAAA
ENST00000359299.7:c.480+80_480+81insAAAAAAAAAAAAAAAAAAAAAA ENSP00000352248.3:n.480+80_480+81insAAAAAAAAAAAAAAAAAAAAAA
ENST00000503003.1:n.86+80_86+81insAAAAAAAAAAAAAAAAAAAAAA
ENST00000507278.5:n.143+80_143+81insAAAAAAAAAAAAAAAAAAAAAA
ENST00000617524.1:c.477+80_477+81insAAAAAAAAAAAAAAAAAAAAAA ENSP00000483710.1:n.477+80_477+81insAAAAAAAAAAAAAAAAAAAAAA
NM_007193.4:c.480+80_480+81insAAAAAAAAAAAAAAAAAAAAAA NP_009124.2:n.480+80_480+81insAAAAAAAAAAAAAAAAAAAAAA
XM_011531571.1:c.540+80_540+81insAAAAAAAAAAAAAAAAAAAAAA XP_011529873.1:n.540+80_540+81insAAAAAAAAAAAAAAAAAAAAAA
XM_011531571.2:c.540+80_540+81insAAAAAAAAAAAAAAAAAAAAAA XP_011529873.1:n.540+80_540+81insAAAAAAAAAAAAAAAAAAAAAA
NM_007193.5:c.480+80_480+81insAAAAAAAAAAAAAAAAAAAAAA MANE Select NP_009124.2:n.480+80_480+81insAAAAAAAAAAAAAAAAAAAAAA