Canonical Allele Identifier: CA2672600753
Gene: ANXA10 HGNC NCBI

Linked Data

dbSNP Id: rs1306712862

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165414G>T , CM000666.2:g.168165414G>T GRCh38
NC_000004.11:g.169086565G>T , CM000666.1:g.169086565G>T GRCh37
NC_000004.10:g.169323140G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+88G>T MANE Select ENSP00000352248.3:n.480+88G>T
ENST00000359299.7:c.480+88G>T ENSP00000352248.3:n.480+88G>T
ENST00000503003.1:n.86+88G>T
ENST00000507278.5:n.143+88G>T
ENST00000617524.1:c.477+88G>T ENSP00000483710.1:n.477+88G>T
NM_007193.4:c.480+88G>T NP_009124.2:n.480+88G>T
XM_011531571.1:c.540+88G>T XP_011529873.1:n.540+88G>T
XM_011531571.2:c.540+88G>T XP_011529873.1:n.540+88G>T
NM_007193.5:c.480+88G>T MANE Select NP_009124.2:n.480+88G>T