Canonical Allele Identifier: CA398844365

Gene: STAC2

Linked Data

• MyVariant Identifiers: chr17:g.37374272G>C (hg19) ; chr17:g.39218019G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39218019G>C , CM000679.2:g.39218019G>C	GRCh38
NC_000017.10:g.37374272G>C , CM000679.1:g.37374272G>C	GRCh37
NC_000017.9:g.34627798G>C	NCBI36
NG_054936.1:g.12769C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333461.6:c.245C>G MANE Select	ENSP00000327509.5:p.Thr82Arg
ENST00000333461.5:c.245C>G	ENSP00000327509.5:p.Thr82Arg
ENST00000584501.1:c.195+50C>G	ENSP00000463299.1:n.195+50C>G
NM_198993.3:c.245C>G	NP_945344.1:p.Thr82Arg
NM_001351360.1:c.-30+50C>G	NP_001338289.1:n.-30+50C>G
NM_198993.4:c.245C>G	NP_945344.1:p.Thr82Arg
XM_017024580.1:c.245C>G	XP_016880069.1:p.Thr82Arg
XM_017024581.1:c.245C>G	XP_016880070.1:p.Thr82Arg
XM_017024583.1:c.245C>G	XP_016880072.1:p.Thr82Arg
XR_002957997.1:n.530C>G
NM_198993.5:c.245C>G MANE Select	NP_945344.1:p.Thr82Arg
NM_001351360.2:c.-30+50C>G	NP_001338289.1:n.-30+50C>G