Canonical Allele Identifier: CA385411087

Gene: STAC3

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332782.7:c.851G>A MANE Select	ENSP00000329200.2:p.Trp284Ter
ENST00000332782.6:c.851G>A	ENSP00000329200.2:p.Trp284Ter
ENST00000546246.2:c.293G>A	ENSP00000441515.2:p.Trp98Ter
ENST00000554578.5:c.734G>A	ENSP00000452068.1:p.Trp245Ter
ENST00000557176.5:c.226G>A	ENSP00000450740.1:p.Gly76Ser
NM_001286256.1:c.734G>A	NP_001273185.1:p.Trp245Ter
NM_001286257.1:c.293G>A	NP_001273186.1:p.Trp98Ter
NM_145064.2:c.851G>A	NP_659501.1:p.Trp284Ter
NR_104422.1:n.553G>A
XM_011538126.1:c.851G>A	XP_011536428.1:p.Trp284Ter
XR_944515.1:n.980G>A
XM_011538126.2:c.851G>A	XP_011536428.1:p.Trp284Ter
XR_002957305.1:n.1150G>A
XR_944515.2:n.980G>A
NM_145064.3:c.851G>A MANE Select	NP_659501.1:p.Trp284Ter
NM_001286256.2:c.734G>A	NP_001273185.1:p.Trp245Ter
NM_001286257.2:c.293G>A	NP_001273186.1:p.Trp98Ter
NR_104422.2:n.547G>A