Canonical Allele Identifier: CA1511397861

Gene: ANXA10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165405_168165407delinsAAT , CM000666.2:g.168165405_168165407delinsAAT	GRCh38
NC_000004.11:g.169086556_169086558delinsAAT , CM000666.1:g.169086556_169086558delinsAAT	GRCh37
NC_000004.10:g.169323131_169323133delinsAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+79_480+81delinsAAT MANE Select	ENSP00000352248.3:n.480+79_480+81delinsAAT
ENST00000359299.7:c.480+79_480+81delinsAAT	ENSP00000352248.3:n.480+79_480+81delinsAAT
ENST00000503003.1:n.86+79_86+81delinsAAT
ENST00000507278.5:n.143+79_143+81delinsAAT
ENST00000617524.1:c.477+79_477+81delinsAAT	ENSP00000483710.1:n.477+79_477+81delinsAAT
NM_007193.4:c.480+79_480+81delinsAAT	NP_009124.2:n.480+79_480+81delinsAAT
XM_011531571.1:c.540+79_540+81delinsAAT	XP_011529873.1:n.540+79_540+81delinsAAT
XM_011531571.2:c.540+79_540+81delinsAAT	XP_011529873.1:n.540+79_540+81delinsAAT
NM_007193.5:c.480+79_480+81delinsAAT MANE Select	NP_009124.2:n.480+79_480+81delinsAAT