Canonical Allele Identifier: CA398844332

Gene: STAC2

Linked Data

• MyVariant Identifiers: chr17:g.37374263T>G (hg19) ; chr17:g.39218010T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39218010T>G , CM000679.2:g.39218010T>G	GRCh38
NC_000017.10:g.37374263T>G , CM000679.1:g.37374263T>G	GRCh37
NC_000017.9:g.34627789T>G	NCBI36
NG_054936.1:g.12778A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333461.6:c.254A>C MANE Select	ENSP00000327509.5:p.Asp85Ala
ENST00000333461.5:c.254A>C	ENSP00000327509.5:p.Asp85Ala
ENST00000584501.1:c.195+59A>C	ENSP00000463299.1:n.195+59A>C
NM_198993.3:c.254A>C	NP_945344.1:p.Asp85Ala
NM_001351360.1:c.-30+59A>C	NP_001338289.1:n.-30+59A>C
NM_198993.4:c.254A>C	NP_945344.1:p.Asp85Ala
XM_017024580.1:c.254A>C	XP_016880069.1:p.Asp85Ala
XM_017024581.1:c.254A>C	XP_016880070.1:p.Asp85Ala
XM_017024583.1:c.254A>C	XP_016880072.1:p.Asp85Ala
XR_002957997.1:n.539A>C
NM_198993.5:c.254A>C MANE Select	NP_945344.1:p.Asp85Ala
NM_001351360.2:c.-30+59A>C	NP_001338289.1:n.-30+59A>C