Canonical Allele Identifier: CA398843932
Gene: STAC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39217908T>A , CM000679.2:g.39217908T>A GRCh38
NC_000017.10:g.37374161T>A , CM000679.1:g.37374161T>A GRCh37
NC_000017.9:g.34627687T>A NCBI36
NG_054936.1:g.12880A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333461.6:c.356A>T MANE Select ENSP00000327509.5:p.Lys119Met
ENST00000333461.5:c.356A>T ENSP00000327509.5:p.Lys119Met
ENST00000584501.1:c.195+161A>T ENSP00000463299.1:n.195+161A>T
NM_198993.3:c.356A>T NP_945344.1:p.Lys119Met
NM_001351360.1:c.-30+161A>T NP_001338289.1:n.-30+161A>T
NM_198993.4:c.356A>T NP_945344.1:p.Lys119Met
XM_017024580.1:c.356A>T XP_016880069.1:p.Lys119Met
XM_017024581.1:c.356A>T XP_016880070.1:p.Lys119Met
XM_017024583.1:c.356A>T XP_016880072.1:p.Lys119Met
XR_002957997.1:n.641A>T
NM_198993.5:c.356A>T MANE Select NP_945344.1:p.Lys119Met
NM_001351360.2:c.-30+161A>T NP_001338289.1:n.-30+161A>T