Canonical Allele Identifier: CA2647330985

Gene: VTCN1

Linked Data

• dbSNP Id: rs2101422090
• gnomAD v4: 1-117147626-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147626G>T , CM000663.2:g.117147626G>T	GRCh38
NC_000001.10:g.117690248G>T , CM000663.1:g.117690248G>T	GRCh37
NC_000001.9:g.117491771G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369458.8:c.*32C>A MANE Select	ENSP00000358470.3:n.*32C>A
ENST00000328189.7:c.*32C>A	ENSP00000328168.3:n.*32C>A
ENST00000359008.8:c.*32C>A	ENSP00000351899.4:n.*32C>A
ENST00000369458.7:c.*32C>A	ENSP00000358470.3:n.*32C>A
ENST00000539893.5:c.*32C>A	ENSP00000444724.1:n.*32C>A
NM_001253849.1:c.*32C>A	NP_001240778.1:n.*32C>A
NM_001253850.1:c.*32C>A	NP_001240779.1:n.*32C>A
NM_024626.3:c.*32C>A	NP_078902.2:n.*32C>A
NR_045603.1:n.1076C>A
NR_045604.1:n.780C>A
XM_011542143.1:c.*32C>A	XP_011540445.1:n.*32C>A
XM_011542144.1:c.*32C>A	XP_011540446.1:n.*32C>A
XM_011542145.1:c.*32C>A	XP_011540447.1:n.*32C>A
XM_011542143.2:c.*32C>A	XP_011540445.2:n.*32C>A
XM_017002335.2:c.*32C>A	XP_016857824.1:n.*32C>A
NM_024626.4:c.*32C>A MANE Select	NP_078902.2:n.*32C>A
NR_045603.2:n.1043C>A
NR_045604.2:n.747C>A
NM_001253849.2:c.*32C>A	NP_001240778.1:n.*32C>A
NM_001253850.2:c.*32C>A	NP_001240779.1:n.*32C>A