Canonical Allele Identifier: CA2546405924

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147735_117147736insATGCAAAGT , CM000663.2:g.117147735_117147736insATGCAAAGT	GRCh38
NC_000001.10:g.117690357_117690358insATGCAAAGT , CM000663.1:g.117690357_117690358insATGCAAAGT	GRCh37
NC_000001.9:g.117491880_117491881insATGCAAAGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.771_772insACTTTGCAT MANE Select	ENSP00000358470.3:p.Lys257_Ala258insThrLeuHis
ENST00000328189.7:c.423_424insACTTTGCAT	ENSP00000328168.3:p.Lys141_Ala142insThrLeuHis
ENST00000359008.8:c.780_781insACTTTGCAT	ENSP00000351899.4:p.Lys260_Ala261insThrLeuHis
ENST00000369458.7:c.771_772insACTTTGCAT	ENSP00000358470.3:p.Lys257_Ala258insThrLeuHis
ENST00000539893.5:c.486_487insACTTTGCAT	ENSP00000444724.1:p.Lys162_Ala163insThrLeuHis
NM_001253849.1:c.486_487insACTTTGCAT	NP_001240778.1:p.Lys162_Ala163insThrLeuHis
NM_001253850.1:c.423_424insACTTTGCAT	NP_001240779.1:p.Lys141_Ala142insThrLeuHis
NM_024626.3:c.771_772insACTTTGCAT	NP_078902.2:p.Lys257_Ala258insThrLeuHis
NR_045603.1:n.966_967insACTTTGCAT
NR_045604.1:n.670_671insACTTTGCAT
XM_011542143.1:c.822_823insACTTTGCAT	XP_011540445.1:p.Lys274_Ala275insThrLeuHis
XM_011542144.1:c.825_826insACTTTGCAT	XP_011540446.1:p.Lys275_Ala276insThrLeuHis
XM_011542145.1:c.786_787insACTTTGCAT	XP_011540447.1:p.Lys262_Ala263insThrLeuHis
XM_011542143.2:c.921_922insACTTTGCAT	XP_011540445.2:p.Lys307_Ala308insThrLeuHis
XM_017002335.2:c.786_787insACTTTGCAT	XP_016857824.1:p.Lys262_Ala263insThrLeuHis
NM_024626.4:c.771_772insACTTTGCAT MANE Select	NP_078902.2:p.Lys257_Ala258insThrLeuHis
NR_045603.2:n.933_934insACTTTGCAT
NR_045604.2:n.637_638insACTTTGCAT
NM_001253849.2:c.486_487insACTTTGCAT	NP_001240778.1:p.Lys162_Ala163insThrLeuHis
NM_001253850.2:c.423_424insACTTTGCAT	NP_001240779.1:p.Lys141_Ala142insThrLeuHis