Canonical Allele Identifier: CA1511397919

Gene: ANXA10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165544_168165545delinsCA , CM000666.2:g.168165544_168165545delinsCA	GRCh38
NC_000004.11:g.169086695_169086696delinsCA , CM000666.1:g.169086695_169086696delinsCA	GRCh37
NC_000004.10:g.169323270_169323271delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+218_480+219delinsCA MANE Select	ENSP00000352248.3:n.480+218_480+219delinsCA
ENST00000359299.7:c.480+218_480+219delinsCA	ENSP00000352248.3:n.480+218_480+219delinsCA
ENST00000503003.1:n.86+218_86+219delinsCA
ENST00000507278.5:n.143+218_143+219delinsCA
ENST00000617524.1:c.477+218_477+219delinsCA	ENSP00000483710.1:n.477+218_477+219delinsCA
NM_007193.4:c.480+218_480+219delinsCA	NP_009124.2:n.480+218_480+219delinsCA
XM_011531571.1:c.540+218_540+219delinsCA	XP_011529873.1:n.540+218_540+219delinsCA
XM_011531571.2:c.540+218_540+219delinsCA	XP_011529873.1:n.540+218_540+219delinsCA
NM_007193.5:c.480+218_480+219delinsCA MANE Select	NP_009124.2:n.480+218_480+219delinsCA