Canonical Allele Identifier: CA917358839

Gene: ANXA10

Linked Data

• dbSNP Id: rs1560788034

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165550del , CM000666.2:g.168165550del	GRCh38
NC_000004.11:g.169086701del , CM000666.1:g.169086701del	GRCh37
NC_000004.10:g.169323276del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+224del MANE Select	ENSP00000352248.3:n.480+224del
ENST00000359299.7:c.480+224del	ENSP00000352248.3:n.480+224del
ENST00000503003.1:n.86+224del
ENST00000507278.5:n.143+224del
ENST00000617524.1:c.477+224del	ENSP00000483710.1:n.477+224del
NM_007193.4:c.480+224del	NP_009124.2:n.480+224del
XM_011531571.1:c.540+224del	XP_011529873.1:n.540+224del
XM_011531571.2:c.540+224del	XP_011529873.1:n.540+224del
NM_007193.5:c.480+224del MANE Select	NP_009124.2:n.480+224del