Canonical Allele Identifier: CA343610503
Gene: STX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180993414A>C , CM000663.2:g.180993414A>C GRCh38
NC_000001.10:g.180962550A>C , CM000663.1:g.180962550A>C GRCh37
NC_000001.9:g.179229173A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000258301.6:c.312T>G MANE Select ENSP00000258301.5:p.Asp104Glu
ENST00000258301.5:c.312T>G ENSP00000258301.5:p.Asp104Glu
ENST00000542060.5:c.9T>G ENSP00000440188.1:p.Asp3Glu
NM_001286210.1:c.9T>G NP_001273139.1:p.Asp3Glu
NM_005819.5:c.312T>G NP_005810.1:p.Asp104Glu
XM_011509058.1:c.312T>G XP_011507360.1:p.Asp104Glu
XM_011509059.1:c.9T>G XP_011507361.1:p.Asp3Glu
XM_017000007.1:c.9T>G XP_016855496.1:p.Asp3Glu
NM_005819.6:c.312T>G MANE Select NP_005810.1:p.Asp104Glu
NM_001286210.2:c.9T>G NP_001273139.1:p.Asp3Glu