Canonical Allele Identifier: CA1511397865

Gene: ANXA10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165406_168165409delinsATAG , CM000666.2:g.168165406_168165409delinsATAG	GRCh38
NC_000004.11:g.169086557_169086560delinsATAG , CM000666.1:g.169086557_169086560delinsATAG	GRCh37
NC_000004.10:g.169323132_169323135delinsATAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+80_480+83delinsATAG MANE Select	ENSP00000352248.3:n.480+80_480+83delinsATAG
ENST00000359299.7:c.480+80_480+83delinsATAG	ENSP00000352248.3:n.480+80_480+83delinsATAG
ENST00000503003.1:n.86+80_86+83delinsATAG
ENST00000507278.5:n.143+80_143+83delinsATAG
ENST00000617524.1:c.477+80_477+83delinsATAG	ENSP00000483710.1:n.477+80_477+83delinsATAG
NM_007193.4:c.480+80_480+83delinsATAG	NP_009124.2:n.480+80_480+83delinsATAG
XM_011531571.1:c.540+80_540+83delinsATAG	XP_011529873.1:n.540+80_540+83delinsATAG
XM_011531571.2:c.540+80_540+83delinsATAG	XP_011529873.1:n.540+80_540+83delinsATAG
NM_007193.5:c.480+80_480+83delinsATAG MANE Select	NP_009124.2:n.480+80_480+83delinsATAG