Canonical Allele Identifier: CA1591252421

Gene: ANXA6

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151126011C= , CM000667.2:g.151126011C=	GRCh38
NC_000005.9:g.150505572C= , CM000667.1:g.150505572C=	GRCh37
NC_000005.8:g.150485765C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000700367.1:c.1056+391G=	ENSP00000514965.1:n.1056+391G=
ENST00000354546.10:c.1056+391G= MANE Select	ENSP00000346550.5:n.1056+391G=
ENST00000354546.9:c.1056+391G=	ENSP00000346550.5:n.1056+391G=
ENST00000377751.9:c.205-3751G=	ENSP00000366980.5:n.205-3751G=
ENST00000517486.5:c.318+12667G=	ENSP00000428916.1:n.318+12667G=
ENST00000519644.6:c.*19+391G=	ENSP00000430663.2:n.*19+391G=
ENST00000520054.1:n.270+391G=
ENST00000521512.5:c.435+391G=	ENSP00000430420.1:n.435+391G=
ENST00000523714.5:c.960+391G=	ENSP00000430517.1:n.960+391G=
NM_001155.4:c.1056+391G=	NP_001146.2:n.1056+391G=
NM_001193544.1:c.960+391G=	NP_001180473.1:n.960+391G=
XM_005268432.3:c.1056+391G=	XP_005268489.1:n.1056+391G=
NM_001363114.1:c.1056+391G=	NP_001350043.1:n.1056+391G=
NM_001155.5:c.1056+391G= MANE Select	NP_001146.2:n.1056+391G=
NM_001193544.2:c.960+391G=	NP_001180473.1:n.960+391G=
NM_001363114.2:c.1056+391G=	NP_001350043.1:n.1056+391G=