Canonical Allele Identifier: CA2038786401

Gene: STAC3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57244322C= , CM000674.2:g.57244322C=	GRCh38
NC_000012.11:g.57638105C= , CM000674.1:g.57638105C=	GRCh37
NC_000012.10:g.55924372C=	NCBI36
NG_033835.1:g.11872G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332782.7:c.851G= MANE Select	ENSP00000329200.2:p.Trp284=
ENST00000332782.6:c.851G=	ENSP00000329200.2:p.Trp284=
ENST00000546246.2:c.293G=	ENSP00000441515.2:p.Trp98=
ENST00000554578.5:c.734G=	ENSP00000452068.1:p.Trp245=
ENST00000557176.5:c.226G=	ENSP00000450740.1:p.Gly76=
NM_001286256.1:c.734G=	NP_001273185.1:p.Trp245=
NM_001286257.1:c.293G=	NP_001273186.1:p.Trp98=
NM_145064.2:c.851G=	NP_659501.1:p.Trp284=
NR_104422.1:n.553G=
XM_011538126.1:c.851G=	XP_011536428.1:p.Trp284=
XR_944515.1:n.980G=
XM_011538126.2:c.851G=	XP_011536428.1:p.Trp284=
XR_002957305.1:n.1150G=
XR_944515.2:n.980G=
NM_145064.3:c.851G= MANE Select	NP_659501.1:p.Trp284=
NM_001286256.2:c.734G=	NP_001273185.1:p.Trp245=
NM_001286257.2:c.293G=	NP_001273186.1:p.Trp98=
NR_104422.2:n.547G=