Canonical Allele Identifier: CA499649919

Gene: STAC2

Linked Data

• MyVariant Identifiers: chr17:g.37374271T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39218018T>A , CM000679.2:g.39218018T>A	GRCh38
NC_000017.10:g.37374271T>A , CM000679.1:g.37374271T>A	GRCh37
NC_000017.9:g.34627797T>A	NCBI36
NG_054936.1:g.12770A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333461.6:c.246A>T MANE Select	ENSP00000327509.5:p.Thr82=
ENST00000333461.5:c.246A>T	ENSP00000327509.5:p.Thr82=
ENST00000584501.1:c.195+51A>T	ENSP00000463299.1:n.195+51A>T
NM_198993.3:c.246A>T	NP_945344.1:p.Thr82=
NM_001351360.1:c.-30+51A>T	NP_001338289.1:n.-30+51A>T
NM_198993.4:c.246A>T	NP_945344.1:p.Thr82=
XM_017024580.1:c.246A>T	XP_016880069.1:p.Thr82=
XM_017024581.1:c.246A>T	XP_016880070.1:p.Thr82=
XM_017024583.1:c.246A>T	XP_016880072.1:p.Thr82=
XR_002957997.1:n.531A>T
NM_198993.5:c.246A>T MANE Select	NP_945344.1:p.Thr82=
NM_001351360.2:c.-30+51A>T	NP_001338289.1:n.-30+51A>T