Canonical Allele Identifier: CA2672600765
Gene: ANXA10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165424G>A , CM000666.2:g.168165424G>A GRCh38
NC_000004.11:g.169086575G>A , CM000666.1:g.169086575G>A GRCh37
NC_000004.10:g.169323150G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+98G>A MANE Select ENSP00000352248.3:n.480+98G>A
ENST00000359299.7:c.480+98G>A ENSP00000352248.3:n.480+98G>A
ENST00000503003.1:n.86+98G>A
ENST00000507278.5:n.143+98G>A
ENST00000617524.1:c.477+98G>A ENSP00000483710.1:n.477+98G>A
NM_007193.4:c.480+98G>A NP_009124.2:n.480+98G>A
XM_011531571.1:c.540+98G>A XP_011529873.1:n.540+98G>A
XM_011531571.2:c.540+98G>A XP_011529873.1:n.540+98G>A
NM_007193.5:c.480+98G>A MANE Select NP_009124.2:n.480+98G>A