Canonical Allele Identifier: CA1591252369

Gene: ANXA6

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151125906G= , CM000667.2:g.151125906G=	GRCh38
NC_000005.9:g.150505467G= , CM000667.1:g.150505467G=	GRCh37
NC_000005.8:g.150485660G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000700367.1:c.1056+496C=	ENSP00000514965.1:n.1056+496C=
ENST00000354546.10:c.1056+496C= MANE Select	ENSP00000346550.5:n.1056+496C=
ENST00000354546.9:c.1056+496C=	ENSP00000346550.5:n.1056+496C=
ENST00000377751.9:c.205-3646C=	ENSP00000366980.5:n.205-3646C=
ENST00000517486.5:c.318+12772C=	ENSP00000428916.1:n.318+12772C=
ENST00000519644.6:c.*19+496C=	ENSP00000430663.2:n.*19+496C=
ENST00000520054.1:n.270+496C=
ENST00000521512.5:c.435+496C=	ENSP00000430420.1:n.435+496C=
ENST00000523714.5:c.960+496C=	ENSP00000430517.1:n.960+496C=
NM_001155.4:c.1056+496C=	NP_001146.2:n.1056+496C=
NM_001193544.1:c.960+496C=	NP_001180473.1:n.960+496C=
XM_005268432.3:c.1056+496C=	XP_005268489.1:n.1056+496C=
NM_001363114.1:c.1056+496C=	NP_001350043.1:n.1056+496C=
NM_001155.5:c.1056+496C= MANE Select	NP_001146.2:n.1056+496C=
NM_001193544.2:c.960+496C=	NP_001180473.1:n.960+496C=
NM_001363114.2:c.1056+496C=	NP_001350043.1:n.1056+496C=