Canonical Allele Identifier: CA8529393

Gene: STAC2

Linked Data

• dbSNP Id: rs377056928
• ExAC: 17:37374163 G / A
• gnomAD v2: 17-37374163-G-A
• gnomAD v3: 17-39217910-G-A
• gnomAD v4: 17-39217910-G-A
• MyVariant Identifiers: chr17:g.37374163G>A (hg19) ; chr17:g.39217910G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39217910G>A , CM000679.2:g.39217910G>A	GRCh38
NC_000017.10:g.37374163G>A , CM000679.1:g.37374163G>A	GRCh37
NC_000017.9:g.34627689G>A	NCBI36
NG_054936.1:g.12878C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000333461.6:c.354C>T MANE Select	ENSP00000327509.5:p.Phe118=
ENST00000333461.5:c.354C>T	ENSP00000327509.5:p.Phe118=
ENST00000584501.1:c.195+159C>T	ENSP00000463299.1:n.195+159C>T
NM_198993.3:c.354C>T	NP_945344.1:p.Phe118=
NM_001351360.1:c.-30+159C>T	NP_001338289.1:n.-30+159C>T
NM_198993.4:c.354C>T	NP_945344.1:p.Phe118=
XM_017024580.1:c.354C>T	XP_016880069.1:p.Phe118=
XM_017024581.1:c.354C>T	XP_016880070.1:p.Phe118=
XM_017024583.1:c.354C>T	XP_016880072.1:p.Phe118=
XR_002957997.1:n.639C>T
NM_198993.5:c.354C>T MANE Select	NP_945344.1:p.Phe118=
NM_001351360.2:c.-30+159C>T	NP_001338289.1:n.-30+159C>T