Canonical Allele Identifier: CA341808052

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690297A>G (hg19) ; chr1:g.117147675A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147675A>G , CM000663.2:g.117147675A>G	GRCh38
NC_000001.10:g.117690297A>G , CM000663.1:g.117690297A>G	GRCh37
NC_000001.9:g.117491820A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.832T>C MANE Select	ENSP00000358470.3:p.Tyr278His
ENST00000328189.7:c.484T>C	ENSP00000328168.3:p.Tyr162His
ENST00000359008.8:c.841T>C	ENSP00000351899.4:p.Tyr281His
ENST00000369458.7:c.832T>C	ENSP00000358470.3:p.Tyr278His
ENST00000539893.5:c.547T>C	ENSP00000444724.1:p.Tyr183His
NM_001253849.1:c.547T>C	NP_001240778.1:p.Tyr183His
NM_001253850.1:c.484T>C	NP_001240779.1:p.Tyr162His
NM_024626.3:c.832T>C	NP_078902.2:p.Tyr278His
NR_045603.1:n.1027T>C
NR_045604.1:n.731T>C
XM_011542143.1:c.883T>C	XP_011540445.1:p.Tyr295His
XM_011542144.1:c.886T>C	XP_011540446.1:p.Tyr296His
XM_011542145.1:c.847T>C	XP_011540447.1:p.Tyr283His
XM_011542143.2:c.982T>C	XP_011540445.2:p.Tyr328His
XM_017002335.2:c.847T>C	XP_016857824.1:p.Tyr283His
NM_024626.4:c.832T>C MANE Select	NP_078902.2:p.Tyr278His
NR_045603.2:n.994T>C
NR_045604.2:n.698T>C
NM_001253849.2:c.547T>C	NP_001240778.1:p.Tyr183His
NM_001253850.2:c.484T>C	NP_001240779.1:p.Tyr162His