Canonical Allele Identifier: CA2502115406

Gene: ANXA10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165585A>G , CM000666.2:g.168165585A>G	GRCh38
NC_000004.11:g.169086736A>G , CM000666.1:g.169086736A>G	GRCh37
NC_000004.10:g.169323311A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+259A>G MANE Select	ENSP00000352248.3:n.480+259A>G
ENST00000359299.7:c.480+259A>G	ENSP00000352248.3:n.480+259A>G
ENST00000503003.1:n.86+259A>G
ENST00000507278.5:n.143+259A>G
ENST00000617524.1:c.477+259A>G	ENSP00000483710.1:n.477+259A>G
NM_007193.4:c.480+259A>G	NP_009124.2:n.480+259A>G
XM_011531571.1:c.540+259A>G	XP_011529873.1:n.540+259A>G
XM_011531571.2:c.540+259A>G	XP_011529873.1:n.540+259A>G
NM_007193.5:c.480+259A>G MANE Select	NP_009124.2:n.480+259A>G