Canonical Allele Identifier: CA341808284

Gene: VTCN1

Linked Data

• dbSNP Id: rs2101423174
• MyVariant Identifiers: chr1:g.117690358C>A (hg19) ; chr1:g.117147736C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147736C>A , CM000663.2:g.117147736C>A	GRCh38
NC_000001.10:g.117690358C>A , CM000663.1:g.117690358C>A	GRCh37
NC_000001.9:g.117491881C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.771G>T MANE Select	ENSP00000358470.3:p.Lys257Asn
ENST00000328189.7:c.423G>T	ENSP00000328168.3:p.Lys141Asn
ENST00000359008.8:c.780G>T	ENSP00000351899.4:p.Lys260Asn
ENST00000369458.7:c.771G>T	ENSP00000358470.3:p.Lys257Asn
ENST00000539893.5:c.486G>T	ENSP00000444724.1:p.Lys162Asn
NM_001253849.1:c.486G>T	NP_001240778.1:p.Lys162Asn
NM_001253850.1:c.423G>T	NP_001240779.1:p.Lys141Asn
NM_024626.3:c.771G>T	NP_078902.2:p.Lys257Asn
NR_045603.1:n.966G>T
NR_045604.1:n.670G>T
XM_011542143.1:c.822G>T	XP_011540445.1:p.Lys274Asn
XM_011542144.1:c.825G>T	XP_011540446.1:p.Lys275Asn
XM_011542145.1:c.786G>T	XP_011540447.1:p.Lys262Asn
XM_011542143.2:c.921G>T	XP_011540445.2:p.Lys307Asn
XM_017002335.2:c.786G>T	XP_016857824.1:p.Lys262Asn
NM_024626.4:c.771G>T MANE Select	NP_078902.2:p.Lys257Asn
NR_045603.2:n.933G>T
NR_045604.2:n.637G>T
NM_001253849.2:c.486G>T	NP_001240778.1:p.Lys162Asn
NM_001253850.2:c.423G>T	NP_001240779.1:p.Lys141Asn