Canonical Allele Identifier: CA419932341

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690307A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147685A>G , CM000663.2:g.117147685A>G	GRCh38
NC_000001.10:g.117690307A>G , CM000663.1:g.117690307A>G	GRCh37
NC_000001.9:g.117491830A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.822T>C MANE Select	ENSP00000358470.3:p.Pro274=
ENST00000328189.7:c.474T>C	ENSP00000328168.3:p.Pro158=
ENST00000359008.8:c.831T>C	ENSP00000351899.4:p.Pro277=
ENST00000369458.7:c.822T>C	ENSP00000358470.3:p.Pro274=
ENST00000539893.5:c.537T>C	ENSP00000444724.1:p.Pro179=
NM_001253849.1:c.537T>C	NP_001240778.1:p.Pro179=
NM_001253850.1:c.474T>C	NP_001240779.1:p.Pro158=
NM_024626.3:c.822T>C	NP_078902.2:p.Pro274=
NR_045603.1:n.1017T>C
NR_045604.1:n.721T>C
XM_011542143.1:c.873T>C	XP_011540445.1:p.Pro291=
XM_011542144.1:c.876T>C	XP_011540446.1:p.Pro292=
XM_011542145.1:c.837T>C	XP_011540447.1:p.Pro279=
XM_011542143.2:c.972T>C	XP_011540445.2:p.Pro324=
XM_017002335.2:c.837T>C	XP_016857824.1:p.Pro279=
NM_024626.4:c.822T>C MANE Select	NP_078902.2:p.Pro274=
NR_045603.2:n.984T>C
NR_045604.2:n.688T>C
NM_001253849.2:c.537T>C	NP_001240778.1:p.Pro179=
NM_001253850.2:c.474T>C	NP_001240779.1:p.Pro158=