Canonical Allele Identifier: CA1511397860

Gene: ANXA10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165404_168165407delinsAAAT , CM000666.2:g.168165404_168165407delinsAAAT	GRCh38
NC_000004.11:g.169086555_169086558delinsAAAT , CM000666.1:g.169086555_169086558delinsAAAT	GRCh37
NC_000004.10:g.169323130_169323133delinsAAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+78_480+81delinsAAAT MANE Select	ENSP00000352248.3:n.480+78_480+81delinsAAAT
ENST00000359299.7:c.480+78_480+81delinsAAAT	ENSP00000352248.3:n.480+78_480+81delinsAAAT
ENST00000503003.1:n.86+78_86+81delinsAAAT
ENST00000507278.5:n.143+78_143+81delinsAAAT
ENST00000617524.1:c.477+78_477+81delinsAAAT	ENSP00000483710.1:n.477+78_477+81delinsAAAT
NM_007193.4:c.480+78_480+81delinsAAAT	NP_009124.2:n.480+78_480+81delinsAAAT
XM_011531571.1:c.540+78_540+81delinsAAAT	XP_011529873.1:n.540+78_540+81delinsAAAT
XM_011531571.2:c.540+78_540+81delinsAAAT	XP_011529873.1:n.540+78_540+81delinsAAAT
NM_007193.5:c.480+78_480+81delinsAAAT MANE Select	NP_009124.2:n.480+78_480+81delinsAAAT