Canonical Allele Identifier: CA29758482

Gene: VTCN1

Linked Data

• dbSNP Id: rs931924953
• gnomAD v4: 1-117147651-A-C
• MyVariant Identifiers: chr1:g.117690273A>C (hg19) ; chr1:g.117147651A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147651A>C , CM000663.2:g.117147651A>C	GRCh38
NC_000001.10:g.117690273A>C , CM000663.1:g.117690273A>C	GRCh37
NC_000001.9:g.117491796A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369458.8:c.*7T>G MANE Select	ENSP00000358470.3:n.*7T>G
ENST00000328189.7:c.*7T>G	ENSP00000328168.3:n.*7T>G
ENST00000359008.8:c.*7T>G	ENSP00000351899.4:n.*7T>G
ENST00000369458.7:c.*7T>G	ENSP00000358470.3:n.*7T>G
ENST00000539893.5:c.*7T>G	ENSP00000444724.1:n.*7T>G
NM_001253849.1:c.*7T>G	NP_001240778.1:n.*7T>G
NM_001253850.1:c.*7T>G	NP_001240779.1:n.*7T>G
NM_024626.3:c.*7T>G	NP_078902.2:n.*7T>G
NR_045603.1:n.1051T>G
NR_045604.1:n.755T>G
XM_011542143.1:c.*7T>G	XP_011540445.1:n.*7T>G
XM_011542144.1:c.*7T>G	XP_011540446.1:n.*7T>G
XM_011542145.1:c.*7T>G	XP_011540447.1:n.*7T>G
XM_011542143.2:c.*7T>G	XP_011540445.2:n.*7T>G
XM_017002335.2:c.*7T>G	XP_016857824.1:n.*7T>G
NM_024626.4:c.*7T>G MANE Select	NP_078902.2:n.*7T>G
NR_045603.2:n.1018T>G
NR_045604.2:n.722T>G
NM_001253849.2:c.*7T>G	NP_001240778.1:n.*7T>G
NM_001253850.2:c.*7T>G	NP_001240779.1:n.*7T>G