Canonical Allele Identifier: CA398843943
Gene: STAC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39217911A>C , CM000679.2:g.39217911A>C GRCh38
NC_000017.10:g.37374164A>C , CM000679.1:g.37374164A>C GRCh37
NC_000017.9:g.34627690A>C NCBI36
NG_054936.1:g.12877T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333461.6:c.353T>G MANE Select ENSP00000327509.5:p.Phe118Cys
ENST00000333461.5:c.353T>G ENSP00000327509.5:p.Phe118Cys
ENST00000584501.1:c.195+158T>G ENSP00000463299.1:n.195+158T>G
NM_198993.3:c.353T>G NP_945344.1:p.Phe118Cys
NM_001351360.1:c.-30+158T>G NP_001338289.1:n.-30+158T>G
NM_198993.4:c.353T>G NP_945344.1:p.Phe118Cys
XM_017024580.1:c.353T>G XP_016880069.1:p.Phe118Cys
XM_017024581.1:c.353T>G XP_016880070.1:p.Phe118Cys
XM_017024583.1:c.353T>G XP_016880072.1:p.Phe118Cys
XR_002957997.1:n.638T>G
NM_198993.5:c.353T>G MANE Select NP_945344.1:p.Phe118Cys
NM_001351360.2:c.-30+158T>G NP_001338289.1:n.-30+158T>G