Canonical Allele Identifier: CA1511397947

Gene: ANXA10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165593_168165597delinsATAAT , CM000666.2:g.168165593_168165597delinsATAAT	GRCh38
NC_000004.11:g.169086744_169086748delinsATAAT , CM000666.1:g.169086744_169086748delinsATAAT	GRCh37
NC_000004.10:g.169323319_169323323delinsATAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+267_480+271delinsATAAT MANE Select	ENSP00000352248.3:n.480+267_480+271delinsATAAT
ENST00000359299.7:c.480+267_480+271delinsATAAT	ENSP00000352248.3:n.480+267_480+271delinsATAAT
ENST00000503003.1:n.86+267_86+271delinsATAAT
ENST00000507278.5:n.143+267_143+271delinsATAAT
ENST00000617524.1:c.477+267_477+271delinsATAAT	ENSP00000483710.1:n.477+267_477+271delinsATAAT
NM_007193.4:c.480+267_480+271delinsATAAT	NP_009124.2:n.480+267_480+271delinsATAAT
XM_011531571.1:c.540+267_540+271delinsATAAT	XP_011529873.1:n.540+267_540+271delinsATAAT
XM_011531571.2:c.540+267_540+271delinsATAAT	XP_011529873.1:n.540+267_540+271delinsATAAT
NM_007193.5:c.480+267_480+271delinsATAAT MANE Select	NP_009124.2:n.480+267_480+271delinsATAAT