Canonical Allele Identifier: CA1210909164
Gene: STX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180993146A>C , CM000663.2:g.180993146A>C GRCh38
NC_000001.10:g.180962282A>C , CM000663.1:g.180962282A>C GRCh37
NC_000001.9:g.179228905A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000258301.6:c.363+217T>G MANE Select ENSP00000258301.5:n.363+217T>G
ENST00000258301.5:c.363+217T>G ENSP00000258301.5:n.363+217T>G
ENST00000542060.5:c.60+217T>G ENSP00000440188.1:n.60+217T>G
NM_001286210.1:c.60+217T>G NP_001273139.1:n.60+217T>G
NM_005819.5:c.363+217T>G NP_005810.1:n.363+217T>G
XM_011509058.1:c.363+217T>G XP_011507360.1:n.363+217T>G
XM_011509059.1:c.60+217T>G XP_011507361.1:n.60+217T>G
XM_017000007.1:c.60+217T>G XP_016855496.1:n.60+217T>G
NM_005819.6:c.363+217T>G MANE Select NP_005810.1:n.363+217T>G
NM_001286210.2:c.60+217T>G NP_001273139.1:n.60+217T>G