Canonical Allele Identifier: CA341808122

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690319C>G (hg19) ; chr1:g.117147697C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147697C>G , CM000663.2:g.117147697C>G	GRCh38
NC_000001.10:g.117690319C>G , CM000663.1:g.117690319C>G	GRCh37
NC_000001.9:g.117491842C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.810G>C MANE Select	ENSP00000358470.3:p.Trp270Cys
ENST00000328189.7:c.462G>C	ENSP00000328168.3:p.Trp154Cys
ENST00000359008.8:c.819G>C	ENSP00000351899.4:p.Trp273Cys
ENST00000369458.7:c.810G>C	ENSP00000358470.3:p.Trp270Cys
ENST00000539893.5:c.525G>C	ENSP00000444724.1:p.Trp175Cys
NM_001253849.1:c.525G>C	NP_001240778.1:p.Trp175Cys
NM_001253850.1:c.462G>C	NP_001240779.1:p.Trp154Cys
NM_024626.3:c.810G>C	NP_078902.2:p.Trp270Cys
NR_045603.1:n.1005G>C
NR_045604.1:n.709G>C
XM_011542143.1:c.861G>C	XP_011540445.1:p.Trp287Cys
XM_011542144.1:c.864G>C	XP_011540446.1:p.Trp288Cys
XM_011542145.1:c.825G>C	XP_011540447.1:p.Trp275Cys
XM_011542143.2:c.960G>C	XP_011540445.2:p.Trp320Cys
XM_017002335.2:c.825G>C	XP_016857824.1:p.Trp275Cys
NM_024626.4:c.810G>C MANE Select	NP_078902.2:p.Trp270Cys
NR_045603.2:n.972G>C
NR_045604.2:n.676G>C
NM_001253849.2:c.525G>C	NP_001240778.1:p.Trp175Cys
NM_001253850.2:c.462G>C	NP_001240779.1:p.Trp154Cys