Canonical Allele Identifier: CA30282214

Gene: VTCN1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117179265C>G , CM000663.2:g.117179265C>G	GRCh38
NC_000001.10:g.117721887C>G , CM000663.1:g.117721887C>G	GRCh37
NC_000001.9:g.117523410C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.33-9094G>C MANE Select	ENSP00000358470.3:n.33-9094G>C
ENST00000328189.7:c.33-9094G>C	ENSP00000328168.3:n.33-9094G>C
ENST00000369458.7:c.33-9094G>C	ENSP00000358470.3:n.33-9094G>C
ENST00000430871.3:c.33-9094G>C	ENSP00000484316.1:n.33-9094G>C
ENST00000463461.5:n.105-9094G>C
ENST00000488493.1:n.220-9094G>C
ENST00000539893.5:c.-253-9094G>C	ENSP00000444724.1:n.-253-9094G>C
NM_001253849.1:c.-253-9094G>C	NP_001240778.1:n.-253-9094G>C
NM_001253850.1:c.33-9094G>C	NP_001240779.1:n.33-9094G>C
NM_024626.3:c.33-9094G>C	NP_078902.2:n.33-9094G>C
NR_045603.1:n.138-9094G>C
NR_045604.1:n.138-9094G>C
XM_011542143.1:c.83+1155G>C	XP_011540445.1:n.83+1155G>C
XM_011542144.1:c.87-9094G>C	XP_011540446.1:n.87-9094G>C
XM_011542143.2:c.182+1155G>C	XP_011540445.2:n.182+1155G>C
XM_017002335.2:c.-231-7093G>C	XP_016857824.1:n.-231-7093G>C
NM_024626.4:c.33-9094G>C MANE Select	NP_078902.2:n.33-9094G>C
NR_045603.2:n.105-9094G>C
NR_045604.2:n.105-9094G>C
NM_001253849.2:c.-253-9094G>C	NP_001240778.1:n.-253-9094G>C
NM_001253850.2:c.33-9094G>C	NP_001240779.1:n.33-9094G>C