Canonical Allele Identifier: CA2647331053

Gene: VTCN1

Linked Data

• gnomAD v4: 1-117147645-TGGCCGAGGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147646_117147654del , CM000663.2:g.117147646_117147654del	GRCh38
NC_000001.10:g.117690268_117690276del , CM000663.1:g.117690268_117690276del	GRCh37
NC_000001.9:g.117491791_117491799del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369458.8:c.*4_*12del MANE Select	ENSP00000358470.3:n.*4_*12del
ENST00000328189.7:c.*4_*12del	ENSP00000328168.3:n.*4_*12del
ENST00000359008.8:c.*4_*12del	ENSP00000351899.4:n.*4_*12del
ENST00000369458.7:c.*4_*12del	ENSP00000358470.3:n.*4_*12del
ENST00000539893.5:c.*4_*12del	ENSP00000444724.1:n.*4_*12del
NM_001253849.1:c.*4_*12del	NP_001240778.1:n.*4_*12del
NM_001253850.1:c.*4_*12del	NP_001240779.1:n.*4_*12del
NM_024626.3:c.*4_*12del	NP_078902.2:n.*4_*12del
NR_045603.1:n.1048_1056del
NR_045604.1:n.752_760del
XM_011542143.1:c.*4_*12del	XP_011540445.1:n.*4_*12del
XM_011542144.1:c.*4_*12del	XP_011540446.1:n.*4_*12del
XM_011542145.1:c.*4_*12del	XP_011540447.1:n.*4_*12del
XM_011542143.2:c.*4_*12del	XP_011540445.2:n.*4_*12del
XM_017002335.2:c.*4_*12del	XP_016857824.1:n.*4_*12del
NM_024626.4:c.*4_*12del MANE Select	NP_078902.2:n.*4_*12del
NR_045603.2:n.1015_1023del
NR_045604.2:n.719_727del
NM_001253849.2:c.*4_*12del	NP_001240778.1:n.*4_*12del
NM_001253850.2:c.*4_*12del	NP_001240779.1:n.*4_*12del