Canonical Allele Identifier: CA1511397877

Gene: ANXA10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165431_168165432delinsAC , CM000666.2:g.168165431_168165432delinsAC	GRCh38
NC_000004.11:g.169086582_169086583delinsAC , CM000666.1:g.169086582_169086583delinsAC	GRCh37
NC_000004.10:g.169323157_169323158delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+105_480+106delinsAC MANE Select	ENSP00000352248.3:n.480+105_480+106delinsAC
ENST00000359299.7:c.480+105_480+106delinsAC	ENSP00000352248.3:n.480+105_480+106delinsAC
ENST00000503003.1:n.86+105_86+106delinsAC
ENST00000507278.5:n.143+105_143+106delinsAC
ENST00000617524.1:c.477+105_477+106delinsAC	ENSP00000483710.1:n.477+105_477+106delinsAC
NM_007193.4:c.480+105_480+106delinsAC	NP_009124.2:n.480+105_480+106delinsAC
XM_011531571.1:c.540+105_540+106delinsAC	XP_011529873.1:n.540+105_540+106delinsAC
XM_011531571.2:c.540+105_540+106delinsAC	XP_011529873.1:n.540+105_540+106delinsAC
NM_007193.5:c.480+105_480+106delinsAC MANE Select	NP_009124.2:n.480+105_480+106delinsAC