Canonical Allele Identifier: CA341808003

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690283T>G (hg19) ; chr1:g.117147661T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147661T>G , CM000663.2:g.117147661T>G	GRCh38
NC_000001.10:g.117690283T>G , CM000663.1:g.117690283T>G	GRCh37
NC_000001.9:g.117491806T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369458.8:c.846A>C MANE Select	ENSP00000358470.3:p.Lys282Asn
ENST00000328189.7:c.498A>C	ENSP00000328168.3:p.Lys166Asn
ENST00000359008.8:c.855A>C	ENSP00000351899.4:p.Lys285Asn
ENST00000369458.7:c.846A>C	ENSP00000358470.3:p.Lys282Asn
ENST00000539893.5:c.561A>C	ENSP00000444724.1:p.Lys187Asn
NM_001253849.1:c.561A>C	NP_001240778.1:p.Lys187Asn
NM_001253850.1:c.498A>C	NP_001240779.1:p.Lys166Asn
NM_024626.3:c.846A>C	NP_078902.2:p.Lys282Asn
NR_045603.1:n.1041A>C
NR_045604.1:n.745A>C
XM_011542143.1:c.897A>C	XP_011540445.1:p.Lys299Asn
XM_011542144.1:c.900A>C	XP_011540446.1:p.Lys300Asn
XM_011542145.1:c.861A>C	XP_011540447.1:p.Lys287Asn
XM_011542143.2:c.996A>C	XP_011540445.2:p.Lys332Asn
XM_017002335.2:c.861A>C	XP_016857824.1:p.Lys287Asn
NM_024626.4:c.846A>C MANE Select	NP_078902.2:p.Lys282Asn
NR_045603.2:n.1008A>C
NR_045604.2:n.712A>C
NM_001253849.2:c.561A>C	NP_001240778.1:p.Lys187Asn
NM_001253850.2:c.498A>C	NP_001240779.1:p.Lys166Asn