Canonical Allele Identifier: CA2258991578
Gene: STAC2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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