Canonical Allele Identifier: CA1511397880

Gene: ANXA10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165439_168165442delinsATAG , CM000666.2:g.168165439_168165442delinsATAG	GRCh38
NC_000004.11:g.169086590_169086593delinsATAG , CM000666.1:g.169086590_169086593delinsATAG	GRCh37
NC_000004.10:g.169323165_169323168delinsATAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+113_480+116delinsATAG MANE Select	ENSP00000352248.3:n.480+113_480+116delinsATAG
ENST00000359299.7:c.480+113_480+116delinsATAG	ENSP00000352248.3:n.480+113_480+116delinsATAG
ENST00000503003.1:n.86+113_86+116delinsATAG
ENST00000507278.5:n.143+113_143+116delinsATAG
ENST00000617524.1:c.477+113_477+116delinsATAG	ENSP00000483710.1:n.477+113_477+116delinsATAG
NM_007193.4:c.480+113_480+116delinsATAG	NP_009124.2:n.480+113_480+116delinsATAG
XM_011531571.1:c.540+113_540+116delinsATAG	XP_011529873.1:n.540+113_540+116delinsATAG
XM_011531571.2:c.540+113_540+116delinsATAG	XP_011529873.1:n.540+113_540+116delinsATAG
NM_007193.5:c.480+113_480+116delinsATAG MANE Select	NP_009124.2:n.480+113_480+116delinsATAG