Canonical Allele Identifier: CA1210907475

Gene: STX6

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180988826T>C , CM000663.2:g.180988826T>C	GRCh38
NC_000001.10:g.180957962T>C , CM000663.1:g.180957962T>C	GRCh37
NC_000001.9:g.179224585T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258301.6:c.490-481A>G MANE Select	ENSP00000258301.5:n.490-481A>G
ENST00000258301.5:c.490-481A>G	ENSP00000258301.5:n.490-481A>G
ENST00000469135.1:n.552A>G
ENST00000542060.5:c.187-481A>G	ENSP00000440188.1:n.187-481A>G
NM_001286210.1:c.187-481A>G	NP_001273139.1:n.187-481A>G
NM_005819.5:c.490-481A>G	NP_005810.1:n.490-481A>G
XM_011509058.1:c.490-481A>G	XP_011507360.1:n.490-481A>G
XM_011509059.1:c.187-481A>G	XP_011507361.1:n.187-481A>G
XM_017000007.1:c.187-481A>G	XP_016855496.1:n.187-481A>G
NM_005819.6:c.490-481A>G MANE Select	NP_005810.1:n.490-481A>G
NM_001286210.2:c.187-481A>G	NP_001273139.1:n.187-481A>G