Canonical Allele Identifier: CA2575973880

Gene: STX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30993253_30993255del , CM000678.2:g.30993253_30993255del	GRCh38
NC_000016.9:g.31004574_31004576del , CM000678.1:g.31004574_31004576del	GRCh37
NC_000016.8:g.30912075_30912077del	NCBI36
NG_041829.1:g.22257_22259del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.676-12_676-10del MANE Select	ENSP00000215095.5:n.676-12_676-10del
ENST00000565419.2:c.676-12_676-10del	ENSP00000455899.1:n.676-12_676-10del
ENST00000215095.9:c.676-12_676-10del	ENSP00000215095.5:n.676-12_676-10del
ENST00000565419.1:c.676-12_676-10del	ENSP00000455899.1:n.676-12_676-10del
ENST00000569638.5:c.424-12_424-10del	ENSP00000457067.1:n.424-12_424-10del
NM_052874.4:c.676-12_676-10del	NP_443106.1:n.676-12_676-10del
XM_017022893.1:c.658-12_658-10del	XP_016878382.1:n.658-12_658-10del
NM_052874.5:c.676-12_676-10del MANE Select	NP_443106.1:n.676-12_676-10del