Canonical Allele Identifier: CA1591241159

Gene: ANXA6

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151101114_151101116delinsCAG , CM000667.2:g.151101114_151101116delinsCAG	GRCh38
NC_000005.9:g.150480675_150480677delinsCAG , CM000667.1:g.150480675_150480677delinsCAG	GRCh37
NC_000005.8:g.150460868_150460870delinsCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354546.10:c.*332_*334delinsCTG MANE Select	ENSP00000346550.5:n.*332_*334delinsCTG
ENST00000354546.9:c.*332_*334delinsCTG	ENSP00000346550.5:n.*332_*334delinsCTG
ENST00000377751.9:c.*332_*334delinsCTG	ENSP00000366980.5:n.*332_*334delinsCTG
ENST00000522664.5:c.201-154_201-152delinsCTG
ENST00000523714.5:c.*332_*334delinsCTG	ENSP00000430517.1:n.*332_*334delinsCTG
NM_001155.4:c.*332_*334delinsCTG	NP_001146.2:n.*332_*334delinsCTG
NM_001193544.1:c.*332_*334delinsCTG	NP_001180473.1:n.*332_*334delinsCTG
XM_005268432.3:c.*332_*334delinsCTG	XP_005268489.1:n.*332_*334delinsCTG
NM_001363114.1:c.*332_*334delinsCTG	NP_001350043.1:n.*332_*334delinsCTG
NM_001155.5:c.*332_*334delinsCTG MANE Select	NP_001146.2:n.*332_*334delinsCTG
NM_001193544.2:c.*332_*334delinsCTG	NP_001180473.1:n.*332_*334delinsCTG
NM_001363114.2:c.*332_*334delinsCTG	NP_001350043.1:n.*332_*334delinsCTG