Canonical Allele Identifier: CA2216836222

Gene: STX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30993291_30993292delinsAG , CM000678.2:g.30993291_30993292delinsAG	GRCh38
NC_000016.9:g.31004612_31004613delinsAG , CM000678.1:g.31004612_31004613delinsAG	GRCh37
NC_000016.8:g.30912113_30912114delinsAG	NCBI36
NG_041829.1:g.22217_22218delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.676-52_676-51delinsCT MANE Select	ENSP00000215095.5:n.676-52_676-51delinsCT
ENST00000565419.2:c.676-52_676-51delinsCT	ENSP00000455899.1:n.676-52_676-51delinsCT
ENST00000215095.9:c.676-52_676-51delinsCT	ENSP00000215095.5:n.676-52_676-51delinsCT
ENST00000565419.1:c.676-52_676-51delinsCT	ENSP00000455899.1:n.676-52_676-51delinsCT
ENST00000569638.5:c.424-52_424-51delinsCT	ENSP00000457067.1:n.424-52_424-51delinsCT
NM_052874.4:c.676-52_676-51delinsCT	NP_443106.1:n.676-52_676-51delinsCT
XM_017022893.1:c.658-52_658-51delinsCT	XP_016878382.1:n.658-52_658-51delinsCT
NM_052874.5:c.676-52_676-51delinsCT MANE Select	NP_443106.1:n.676-52_676-51delinsCT