Canonical Allele Identifier: CA525459933

Gene: VTCN1

Linked Data

• dbSNP Id: rs1373086221
• gnomAD v2: 1-117690275-G-GTTTTTTTT
• gnomAD v3: 1-117147653-G-GTTTTTTTT
• gnomAD v4: 1-117147653-G-GTTTTTTTT
• MyVariant Identifiers: chr1:g.117690275_117690276insTTTTTTTT (hg19) ; chr1:g.117147653_117147654insTTTTTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147653_117147654insTTTTTTTT , CM000663.2:g.117147653_117147654insTTTTTTTT	GRCh38
NC_000001.10:g.117690275_117690276insTTTTTTTT , CM000663.1:g.117690275_117690276insTTTTTTTT	GRCh37
NC_000001.9:g.117491798_117491799insTTTTTTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.*4_*5insAAAAAAAA MANE Select	ENSP00000358470.3:n.*4_*5insAAAAAAAA
ENST00000328189.7:c.*4_*5insAAAAAAAA	ENSP00000328168.3:n.*4_*5insAAAAAAAA
ENST00000359008.8:c.*4_*5insAAAAAAAA	ENSP00000351899.4:n.*4_*5insAAAAAAAA
ENST00000369458.7:c.*4_*5insAAAAAAAA	ENSP00000358470.3:n.*4_*5insAAAAAAAA
ENST00000539893.5:c.*4_*5insAAAAAAAA	ENSP00000444724.1:n.*4_*5insAAAAAAAA
NM_001253849.1:c.*4_*5insAAAAAAAA	NP_001240778.1:n.*4_*5insAAAAAAAA
NM_001253850.1:c.*4_*5insAAAAAAAA	NP_001240779.1:n.*4_*5insAAAAAAAA
NM_024626.3:c.*4_*5insAAAAAAAA	NP_078902.2:n.*4_*5insAAAAAAAA
NR_045603.1:n.1048_1049insAAAAAAAA
NR_045604.1:n.752_753insAAAAAAAA
XM_011542143.1:c.*4_*5insAAAAAAAA	XP_011540445.1:n.*4_*5insAAAAAAAA
XM_011542144.1:c.*4_*5insAAAAAAAA	XP_011540446.1:n.*4_*5insAAAAAAAA
XM_011542145.1:c.*4_*5insAAAAAAAA	XP_011540447.1:n.*4_*5insAAAAAAAA
XM_011542143.2:c.*4_*5insAAAAAAAA	XP_011540445.2:n.*4_*5insAAAAAAAA
XM_017002335.2:c.*4_*5insAAAAAAAA	XP_016857824.1:n.*4_*5insAAAAAAAA
NM_024626.4:c.*4_*5insAAAAAAAA MANE Select	NP_078902.2:n.*4_*5insAAAAAAAA
NR_045603.2:n.1015_1016insAAAAAAAA
NR_045604.2:n.719_720insAAAAAAAA
NM_001253849.2:c.*4_*5insAAAAAAAA	NP_001240778.1:n.*4_*5insAAAAAAAA
NM_001253850.2:c.*4_*5insAAAAAAAA	NP_001240779.1:n.*4_*5insAAAAAAAA