Canonical Allele Identifier: CA341808077

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690305A>T (hg19) ; chr1:g.117147683A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147683A>T , CM000663.2:g.117147683A>T	GRCh38
NC_000001.10:g.117690305A>T , CM000663.1:g.117690305A>T	GRCh37
NC_000001.9:g.117491828A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.824T>A MANE Select	ENSP00000358470.3:p.Leu275His
ENST00000328189.7:c.476T>A	ENSP00000328168.3:p.Leu159His
ENST00000359008.8:c.833T>A	ENSP00000351899.4:p.Leu278His
ENST00000369458.7:c.824T>A	ENSP00000358470.3:p.Leu275His
ENST00000539893.5:c.539T>A	ENSP00000444724.1:p.Leu180His
NM_001253849.1:c.539T>A	NP_001240778.1:p.Leu180His
NM_001253850.1:c.476T>A	NP_001240779.1:p.Leu159His
NM_024626.3:c.824T>A	NP_078902.2:p.Leu275His
NR_045603.1:n.1019T>A
NR_045604.1:n.723T>A
XM_011542143.1:c.875T>A	XP_011540445.1:p.Leu292His
XM_011542144.1:c.878T>A	XP_011540446.1:p.Leu293His
XM_011542145.1:c.839T>A	XP_011540447.1:p.Leu280His
XM_011542143.2:c.974T>A	XP_011540445.2:p.Leu325His
XM_017002335.2:c.839T>A	XP_016857824.1:p.Leu280His
NM_024626.4:c.824T>A MANE Select	NP_078902.2:p.Leu275His
NR_045603.2:n.986T>A
NR_045604.2:n.690T>A
NM_001253849.2:c.539T>A	NP_001240778.1:p.Leu180His
NM_001253850.2:c.476T>A	NP_001240779.1:p.Leu159His