Canonical Allele Identifier: CA15124559
Gene: VTCN1 HGNC NCBI

Linked Data

dbSNP Id: rs12046117

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.117208743C>T , CM000663.2:g.117208743C>T GRCh38
NC_000001.10:g.117751365C>T , CM000663.1:g.117751365C>T GRCh37
NC_000001.9:g.117552888C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369458.8:c.32+2081G>A MANE Select ENSP00000358470.3:n.32+2081G>A
ENST00000328189.7:c.32+2081G>A ENSP00000328168.3:n.32+2081G>A
ENST00000369458.7:c.32+2081G>A ENSP00000358470.3:n.32+2081G>A
ENST00000430871.3:c.32+2081G>A ENSP00000484316.1:n.32+2081G>A
ENST00000463461.5:n.104+2081G>A
NM_001253850.1:c.32+2081G>A NP_001240779.1:n.32+2081G>A
NM_024626.3:c.32+2081G>A NP_078902.2:n.32+2081G>A
NR_045603.1:n.137+2081G>A
NR_045604.1:n.137+2081G>A
XM_011542144.1:c.87-38572G>A XP_011540446.1:n.87-38572G>A
XM_017002335.2:c.-232+2081G>A XP_016857824.1:n.-232+2081G>A
NM_024626.4:c.32+2081G>A MANE Select NP_078902.2:n.32+2081G>A
NR_045603.2:n.104+2081G>A
NR_045604.2:n.104+2081G>A
NM_001253850.2:c.32+2081G>A NP_001240779.1:n.32+2081G>A