Canonical Allele Identifier: CA2672600743

Gene: ANXA10

Linked Data

• gnomAD v4: 4-168165406-A-AAAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165406_168165407insAAAG , CM000666.2:g.168165406_168165407insAAAG	GRCh38
NC_000004.11:g.169086557_169086558insAAAG , CM000666.1:g.169086557_169086558insAAAG	GRCh37
NC_000004.10:g.169323132_169323133insAAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+80_480+81insAAAG MANE Select	ENSP00000352248.3:n.480+80_480+81insAAAG
ENST00000359299.7:c.480+80_480+81insAAAG	ENSP00000352248.3:n.480+80_480+81insAAAG
ENST00000503003.1:n.86+80_86+81insAAAG
ENST00000507278.5:n.143+80_143+81insAAAG
ENST00000617524.1:c.477+80_477+81insAAAG	ENSP00000483710.1:n.477+80_477+81insAAAG
NM_007193.4:c.480+80_480+81insAAAG	NP_009124.2:n.480+80_480+81insAAAG
XM_011531571.1:c.540+80_540+81insAAAG	XP_011529873.1:n.540+80_540+81insAAAG
XM_011531571.2:c.540+80_540+81insAAAG	XP_011529873.1:n.540+80_540+81insAAAG
NM_007193.5:c.480+80_480+81insAAAG MANE Select	NP_009124.2:n.480+80_480+81insAAAG