Canonical Allele Identifier: CA1919908932

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74119557_74119558delinsTG , CM000672.2:g.74119557_74119558delinsTG	GRCh38
NC_000010.10:g.75879315_75879316delinsTG , CM000672.1:g.75879315_75879316delinsTG	GRCh37
NC_000010.9:g.75549321_75549322delinsTG	NCBI36
NG_008868.1:g.126444_126445delinsTG , LRG_383:g.126444_126445delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.*1388_*1389delinsTG MANE Select	ENSP00000211998.5:n.*1388_*1389delinsTG
ENST00000211998.8:c.*1388_*1389delinsTG	ENSP00000211998.4:n.*1388_*1389delinsTG
ENST00000372755.7:c.*1388_*1389delinsTG	ENSP00000361841.3:n.*1388_*1389delinsTG
ENST00000436396.1:c.3809_3810delinsTG	ENSP00000415489.1:n.3809_3810delinsTG
ENST00000623461.3:n.7392_7393delinsTG
NM_003373.3:c.*1388_*1389delinsTG	NP_003364.1:n.*1388_*1389delinsTG
NM_014000.2:c.*1388_*1389delinsTG , LRG_383t1:c.*1388_*1389delinsTG	NP_054706.1:n.*1388_*1389delinsTG
XM_005270142.1:c.*1388_*1389delinsTG	XP_005270199.1:n.*1388_*1389delinsTG
XM_005270143.1:c.*1388_*1389delinsTG	XP_005270200.1:n.*1388_*1389delinsTG
NM_003373.4:c.*1388_*1389delinsTG	NP_003364.1:n.*1388_*1389delinsTG
NM_014000.3:c.*1388_*1389delinsTG MANE Select	NP_054706.1:n.*1388_*1389delinsTG