Canonical Allele Identifier: CA29758583

Gene: VTCN1

Linked Data

• dbSNP Id: rs751451973
• gnomAD v2: 1-117690335-AAAG-A
• gnomAD v3: 1-117147713-AAAG-A
• gnomAD v4: 1-117147713-AAAG-A
• MyVariant Identifiers: chr1:g.117690336_117690338del (hg19) ; chr1:g.117147714_117147716del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147718_117147720del , CM000663.2:g.117147718_117147720del	GRCh38
NC_000001.10:g.117690340_117690342del , CM000663.1:g.117690340_117690342del	GRCh37
NC_000001.9:g.117491863_117491865del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.791_793del MANE Select	ENSP00000358470.3:p.Ser264del
ENST00000328189.7:c.443_445del	ENSP00000328168.3:p.Ser148del
ENST00000359008.8:c.800_802del	ENSP00000351899.4:p.Ser267del
ENST00000369458.7:c.791_793del	ENSP00000358470.3:p.Ser264del
ENST00000539893.5:c.506_508del	ENSP00000444724.1:p.Ser169del
NM_001253849.1:c.506_508del	NP_001240778.1:p.Ser169del
NM_001253850.1:c.443_445del	NP_001240779.1:p.Ser148del
NM_024626.3:c.791_793del	NP_078902.2:p.Ser264del
NR_045603.1:n.986_988del
NR_045604.1:n.690_692del
XM_011542143.1:c.842_844del	XP_011540445.1:p.Ser281del
XM_011542144.1:c.845_847del	XP_011540446.1:p.Ser282del
XM_011542145.1:c.806_808del	XP_011540447.1:p.Ser269del
XM_011542143.2:c.941_943del	XP_011540445.2:p.Ser314del
XM_017002335.2:c.806_808del	XP_016857824.1:p.Ser269del
NM_024626.4:c.791_793del MANE Select	NP_078902.2:p.Ser264del
NR_045603.2:n.953_955del
NR_045604.2:n.657_659del
NM_001253849.2:c.506_508del	NP_001240778.1:p.Ser169del
NM_001253850.2:c.443_445del	NP_001240779.1:p.Ser148del