Canonical Allele Identifier: CA383558659

Gene: VAMP1 TAPBPL

Linked Data

• ClinVar Variation Id: 1806955
• ClinVar RCV Id: RCV002474384 ; RCV002571516
• MyVariant Identifiers: chr12:g.6574054A>T (hg19) ; chr12:g.6464888A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6464888A>T , CM000674.2:g.6464888A>T	GRCh38
NC_000012.11:g.6574054A>T , CM000674.1:g.6574054A>T	GRCh37
NC_000012.10:g.6444315A>T	NCBI36
NG_042188.1:g.11012T>A
NG_042188.2:g.11012T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361716.8:c.342T>A (VAMP1)	ENSP00000355122.3:p.Ser114Arg
ENST00000396308.4:c.340+2T>A (VAMP1) MANE Select	ENSP00000379602.3:n.340+2T>A
ENST00000361716.7:c.342T>A (VAMP1)	ENSP00000355122.3:p.Ser114Arg
ENST00000396308.3:c.340+2T>A (VAMP1)	ENSP00000379602.3:n.340+2T>A
ENST00000400911.7:c.340+2T>A (VAMP1)	ENSP00000383702.3:n.340+2T>A
ENST00000535180.5:c.340+2T>A (VAMP1)	ENSP00000444181.1:n.340+2T>A
ENST00000535927.5:n.361T>A (VAMP1)
ENST00000538970.5:n.261T>A (VAMP1)
ENST00000544432.5:n.296+2T>A (VAMP1)
ENST00000545700.5:n.1702-987A>T (TAPBPL)
NM_001297438.1:c.340+2T>A (VAMP1)	NP_001284367.1:n.340+2T>A
NM_014231.4:c.340+2T>A (VAMP1)	NP_055046.1:n.340+2T>A
NM_016830.3:c.340+2T>A (VAMP1)	NP_058439.1:n.340+2T>A
NM_199245.2:c.342T>A (VAMP1)	NP_954740.1:p.Ser114Arg
NR_123717.1:n.581+2T>A (VAMP1)
XR_001748777.2:n.1679-2163A>T (TAPBPL)
XR_001748778.2:n.1679-2166A>T (TAPBPL)
NM_001297438.2:c.340+2T>A (VAMP1)	NP_001284367.1:n.340+2T>A
NM_014231.5:c.340+2T>A (VAMP1) MANE Select	NP_055046.1:n.340+2T>A
NM_016830.4:c.340+2T>A (VAMP1)	NP_058439.1:n.340+2T>A
NM_199245.3:c.342T>A (VAMP1)	NP_954740.1:p.Ser114Arg
NR_123717.2:n.359+2T>A (VAMP1)