Canonical Allele Identifier: CA294669627

Gene: SEPTIN9

Linked Data

• dbSNP Id: rs372287642
• gnomAD v3: 17-77320209-AGAGGAGGAG-A
• gnomAD v4: 17-77320209-AGAGGAGGAG-A
• MyVariant Identifiers: chr17:g.75316292_75316300del (hg19) ; chr17:g.77320210_77320218del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.77320226_77320234del , CM000679.2:g.77320226_77320234del	GRCh38
NC_000017.10:g.75316308_75316316del , CM000679.1:g.75316308_75316316del	GRCh37
NC_000017.9:g.72827903_72827911del	NCBI36
NG_011683.1:g.43817_43825del
NG_011683.2:g.43817_43825del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329047.13:c.-101_-93del MANE Plus Clinical	ENSP00000329161.8:n.-101_-93del
ENST00000427177.6:c.76+13029_76+13037del MANE Select	ENSP00000391249.1:n.76+13029_76+13037del
ENST00000329047.12:c.-101_-93del	ENSP00000329161.8:n.-101_-93del
ENST00000427177.5:c.76+13029_76+13037del	ENSP00000391249.1:n.76+13029_76+13037del
ENST00000431235.6:c.-417+13029_-417+13037del	ENSP00000406987.2:n.-417+13029_-417+13037del
ENST00000449803.6:c.-417+13029_-417+13037del	ENSP00000400181.2:n.-417+13029_-417+13037del
ENST00000587237.1:n.406+13029_406+13037del
ENST00000588575.1:c.36+423_36+431del	ENSP00000468090.1:n.36+423_36+431del
ENST00000589070.1:c.31+39420_31+39428del	ENSP00000465332.1:n.31+39420_31+39428del
ENST00000590294.5:c.-101_-93del	ENSP00000465464.1:n.-101_-93del
ENST00000590576.5:c.*76+13029_*76+13037del	ENSP00000465600.1:n.*76+13029_*76+13037del
ENST00000590595.1:c.36+423_36+431del	ENSP00000465026.1:n.36+423_36+431del
ENST00000591198.5:c.19+38672_19+38680del	ENSP00000468406.1:n.19+38672_19+38680del
ENST00000591833.5:c.*71+13029_*71+13037del	ENSP00000466684.1:n.*71+13029_*71+13037del
NM_001113491.1:c.76+13029_76+13037del	NP_001106963.1:n.76+13029_76+13037del
NM_001113492.1:c.-417+13029_-417+13037del	NP_001106964.1:n.-417+13029_-417+13037del
NM_001293695.1:c.19+38672_19+38680del	NP_001280624.1:n.19+38672_19+38680del
NM_006640.4:c.-101_-93del	NP_006631.2:n.-101_-93del
XM_006721643.2:c.-417+13029_-417+13037del	XP_006721706.1:n.-417+13029_-417+13037del
XM_011524204.1:c.169+13029_169+13037del	XP_011522506.1:n.169+13029_169+13037del
XM_011524205.1:c.166+13029_166+13037del	XP_011522507.1:n.166+13029_166+13037del
NM_001113491.2:c.76+13029_76+13037del MANE Select	NP_001106963.1:n.76+13029_76+13037del
NM_001293695.2:c.19+38672_19+38680del	NP_001280624.1:n.19+38672_19+38680del
NM_001113492.2:c.-417+13029_-417+13037del	NP_001106964.1:n.-417+13029_-417+13037del
NM_006640.5:c.-101_-93del MANE Plus Clinical	NP_006631.2:n.-101_-93del