Canonical Allele Identifier: CA29758442

Gene: VTCN1

Linked Data

• dbSNP Id: rs35552588
• MyVariant Identifiers: chr1:g.117690254_117690255insC (hg19) ; chr1:g.117147632_117147633insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147633dup , CM000663.2:g.117147633dup	GRCh38
NC_000001.10:g.117690255dup , CM000663.1:g.117690255dup	GRCh37
NC_000001.9:g.117491778dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369458.8:c.*25dup MANE Select	ENSP00000358470.3:n.*25dup
ENST00000328189.7:c.*25dup	ENSP00000328168.3:n.*25dup
ENST00000359008.8:c.*25dup	ENSP00000351899.4:n.*25dup
ENST00000369458.7:c.*25dup	ENSP00000358470.3:n.*25dup
ENST00000539893.5:c.*25dup	ENSP00000444724.1:n.*25dup
NM_001253849.1:c.*25dup	NP_001240778.1:n.*25dup
NM_001253850.1:c.*25dup	NP_001240779.1:n.*25dup
NM_024626.3:c.*25dup	NP_078902.2:n.*25dup
NR_045603.1:n.1069dup
NR_045604.1:n.773dup
XM_011542143.1:c.*25dup	XP_011540445.1:n.*25dup
XM_011542144.1:c.*25dup	XP_011540446.1:n.*25dup
XM_011542145.1:c.*25dup	XP_011540447.1:n.*25dup
XM_011542143.2:c.*25dup	XP_011540445.2:n.*25dup
XM_017002335.2:c.*25dup	XP_016857824.1:n.*25dup
NM_024626.4:c.*25dup MANE Select	NP_078902.2:n.*25dup
NR_045603.2:n.1036dup
NR_045604.2:n.740dup
NM_001253849.2:c.*25dup	NP_001240778.1:n.*25dup
NM_001253850.2:c.*25dup	NP_001240779.1:n.*25dup