Canonical Allele Identifier: CA2676049908

Gene: ANXA6

Linked Data

• gnomAD v4: 5-151101121-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151101122del , CM000667.2:g.151101122del	GRCh38
NC_000005.9:g.150480683del , CM000667.1:g.150480683del	GRCh37
NC_000005.8:g.150460876del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354546.10:c.*326del MANE Select	ENSP00000346550.5:n.*326del
ENST00000354546.9:c.*326del	ENSP00000346550.5:n.*326del
ENST00000377751.9:c.*326del	ENSP00000366980.5:n.*326del
ENST00000522664.5:c.201-160del
ENST00000523714.5:c.*326del	ENSP00000430517.1:n.*326del
NM_001155.4:c.*326del	NP_001146.2:n.*326del
NM_001193544.1:c.*326del	NP_001180473.1:n.*326del
XM_005268432.3:c.*326del	XP_005268489.1:n.*326del
NM_001363114.1:c.*326del	NP_001350043.1:n.*326del
NM_001155.5:c.*326del MANE Select	NP_001146.2:n.*326del
NM_001193544.2:c.*326del	NP_001180473.1:n.*326del
NM_001363114.2:c.*326del	NP_001350043.1:n.*326del