Canonical Allele Identifier: CA2246776399

Gene: STX8

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.9433053G= , CM000679.2:g.9433053G=	GRCh38
NC_000017.10:g.9336370G= , CM000679.1:g.9336370G=	GRCh37
NC_000017.9:g.9277095G=	NCBI36
NG_047110.1:g.147906C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004853.3:c.542-54400C= MANE Select	NP_004844.1:n.542-54400C=
ENST00000306357.9:c.542-54400C= MANE Select	ENSP00000305255.2:n.542-54400C=
NM_004853.2:c.542-54400C=	NP_004844.1:n.542-54400C=
NR_033656.1:n.486-54400C=
NR_033656.2:n.348-54400C=
ENST00000306357.8:c.542-54400C=	ENSP00000305255.2:n.542-54400C=
ENST00000570583.5:n.93+4744C=
ENST00000574431.5:c.209-54400C=	ENSP00000467749.1:n.209-54400C=
ENST00000574775.1:n.38-54400C=
ENST00000575294.6:c.*55-54400C=	ENSP00000468093.1:n.*55-54400C=
ENST00000575858.5:c.*201-54400C=	ENSP00000460355.1:n.*201-54400C=
XM_011524079.1:c.377-54400C=	XP_011522381.1:n.377-54400C=
XM_011524079.2:c.377-54400C=	XP_011522381.1:n.377-54400C=
XR_934120.1:n.718+4744C=
XR_934120.2:n.718+4744C=