Canonical Allele Identifier: CA1070710757
Gene: ANXA10 HGNC NCBI

Linked Data

dbSNP Id: rs1731859973

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165412_168165416del , CM000666.2:g.168165412_168165416del GRCh38
NC_000004.11:g.169086563_169086567del , CM000666.1:g.169086563_169086567del GRCh37
NC_000004.10:g.169323138_169323142del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+86_480+90del MANE Select ENSP00000352248.3:n.480+86_480+90del
ENST00000359299.7:c.480+86_480+90del ENSP00000352248.3:n.480+86_480+90del
ENST00000503003.1:n.86+86_86+90del
ENST00000507278.5:n.143+86_143+90del
ENST00000617524.1:c.477+86_477+90del ENSP00000483710.1:n.477+86_477+90del
NM_007193.4:c.480+86_480+90del NP_009124.2:n.480+86_480+90del
XM_011531571.1:c.540+86_540+90del XP_011529873.1:n.540+86_540+90del
XM_011531571.2:c.540+86_540+90del XP_011529873.1:n.540+86_540+90del
NM_007193.5:c.480+86_480+90del MANE Select NP_009124.2:n.480+86_480+90del