Canonical Allele Identifier: CA2578228344
Gene: ANXA10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165405A>C , CM000666.2:g.168165405A>C GRCh38
NC_000004.11:g.169086556A>C , CM000666.1:g.169086556A>C GRCh37
NC_000004.10:g.169323131A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+79A>C MANE Select ENSP00000352248.3:n.480+79A>C
ENST00000359299.7:c.480+79A>C ENSP00000352248.3:n.480+79A>C
ENST00000503003.1:n.86+79A>C
ENST00000507278.5:n.143+79A>C
ENST00000617524.1:c.477+79A>C ENSP00000483710.1:n.477+79A>C
NM_007193.4:c.480+79A>C NP_009124.2:n.480+79A>C
XM_011531571.1:c.540+79A>C XP_011529873.1:n.540+79A>C
XM_011531571.2:c.540+79A>C XP_011529873.1:n.540+79A>C
NM_007193.5:c.480+79A>C MANE Select NP_009124.2:n.480+79A>C