Canonical Allele Identifier: CA1511397933
Gene: ANXA10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165574_168165578delinsTATAA , CM000666.2:g.168165574_168165578delinsTATAA GRCh38
NC_000004.11:g.169086725_169086729delinsTATAA , CM000666.1:g.169086725_169086729delinsTATAA GRCh37
NC_000004.10:g.169323300_169323304delinsTATAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+248_480+252delinsTATAA MANE Select ENSP00000352248.3:n.480+248_480+252delinsTATAA
ENST00000359299.7:c.480+248_480+252delinsTATAA ENSP00000352248.3:n.480+248_480+252delinsTATAA
ENST00000503003.1:n.86+248_86+252delinsTATAA
ENST00000507278.5:n.143+248_143+252delinsTATAA
ENST00000617524.1:c.477+248_477+252delinsTATAA ENSP00000483710.1:n.477+248_477+252delinsTATAA
NM_007193.4:c.480+248_480+252delinsTATAA NP_009124.2:n.480+248_480+252delinsTATAA
XM_011531571.1:c.540+248_540+252delinsTATAA XP_011529873.1:n.540+248_540+252delinsTATAA
XM_011531571.2:c.540+248_540+252delinsTATAA XP_011529873.1:n.540+248_540+252delinsTATAA
NM_007193.5:c.480+248_480+252delinsTATAA MANE Select NP_009124.2:n.480+248_480+252delinsTATAA