Canonical Allele Identifier: CA365948878

Gene: STX11

Linked Data

• MyVariant Identifiers: chr6:g.144508031C>G (hg19) ; chr6:g.144186894C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.144186894C>G , CM000668.2:g.144186894C>G	GRCh38
NC_000006.11:g.144508031C>G , CM000668.1:g.144508031C>G	GRCh37
NC_000006.10:g.144549724C>G	NCBI36
NG_007613.1:g.41378C>G , LRG_113:g.41378C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698355.1:c.267C>G	ENSP00000513678.1:p.Ile89Met
ENST00000698356.1:c.267C>G	ENSP00000513679.1:p.Ile89Met
ENST00000698357.1:c.267C>G	ENSP00000513680.1:p.Ile89Met
ENST00000367568.5:c.267C>G MANE Select	ENSP00000356540.4:p.Ile89Met
ENST00000367568.4:c.267C>G	ENSP00000356540.4:p.Ile89Met
NM_003764.3:c.267C>G , LRG_113t1:c.267C>G	NP_003755.2:p.Ile89Met
XM_011536213.1:c.345C>G	XP_011534515.1:p.Ile115Met
XM_011536214.1:c.267C>G	XP_011534516.1:p.Ile89Met
XM_011536215.1:c.267C>G	XP_011534517.1:p.Ile89Met
XM_011536216.1:c.267C>G	XP_011534518.1:p.Ile89Met
XM_011536217.1:c.267C>G	XP_011534519.1:p.Ile89Met
XM_011536218.1:c.267C>G	XP_011534520.1:p.Ile89Met
XM_011536213.2:c.345C>G	XP_011534515.1:p.Ile115Met
XM_011536214.2:c.267C>G	XP_011534516.1:p.Ile89Met
XM_011536217.2:c.267C>G	XP_011534519.1:p.Ile89Met
XM_011536218.2:c.267C>G	XP_011534520.1:p.Ile89Met
XM_017011400.1:c.267C>G	XP_016866889.1:p.Ile89Met
NM_003764.4:c.267C>G MANE Select	NP_003755.2:p.Ile89Met