Canonical Allele Identifier: CA1591241168

Gene: ANXA6

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151101126A= , CM000667.2:g.151101126A=	GRCh38
NC_000005.9:g.150480687A= , CM000667.1:g.150480687A=	GRCh37
NC_000005.8:g.150460880A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700367.1:c.*322T=	ENSP00000514965.1:n.*322T=
ENST00000354546.10:c.*322T= MANE Select	ENSP00000346550.5:n.*322T=
ENST00000354546.9:c.*322T=	ENSP00000346550.5:n.*322T=
ENST00000377751.9:c.*322T=	ENSP00000366980.5:n.*322T=
ENST00000522664.5:c.201-164T=
ENST00000523714.5:c.*322T=	ENSP00000430517.1:n.*322T=
NM_001155.4:c.*322T=	NP_001146.2:n.*322T=
NM_001193544.1:c.*322T=	NP_001180473.1:n.*322T=
XM_005268432.3:c.*322T=	XP_005268489.1:n.*322T=
NM_001363114.1:c.*322T=	NP_001350043.1:n.*322T=
NM_001155.5:c.*322T= MANE Select	NP_001146.2:n.*322T=
NM_001193544.2:c.*322T=	NP_001180473.1:n.*322T=
NM_001363114.2:c.*322T=	NP_001350043.1:n.*322T=