Canonical Allele Identifier: CA1919905127

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74094252_74094256delinsGCTGT , CM000672.2:g.74094252_74094256delinsGCTGT	GRCh38
NC_000010.10:g.75854010_75854014delinsGCTGT , CM000672.1:g.75854010_75854014delinsGCTGT	GRCh37
NC_000010.9:g.75524016_75524020delinsGCTGT	NCBI36
NG_008868.1:g.101139_101143delinsGCTGT , LRG_383:g.101139_101143delinsGCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.1353-19_1353-15delinsGCTGT MANE Select	ENSP00000211998.5:n.1353-19_1353-15delinsGCTGT
ENST00000211998.8:c.1353-19_1353-15delinsGCTGT	ENSP00000211998.4:n.1353-19_1353-15delinsGCTGT
ENST00000372755.7:c.1353-19_1353-15delinsGCTGT	ENSP00000361841.3:n.1353-19_1353-15delinsGCTGT
ENST00000436396.1:c.369-19_369-15delinsGCTGT	ENSP00000415489.1:n.369-19_369-15delinsGCTGT
ENST00000478896.2:n.332-6802_332-6798delinsGCTGT
ENST00000623461.3:n.4156-19_4156-15delinsGCTGT
ENST00000624354.3:c.*1108-19_*1108-15delinsGCTGT	ENSP00000485551.1:n.*1108-19_*1108-15delinsGCTGT
NM_003373.3:c.1353-19_1353-15delinsGCTGT	NP_003364.1:n.1353-19_1353-15delinsGCTGT
NM_014000.2:c.1353-19_1353-15delinsGCTGT , LRG_383t1:c.1353-19_1353-15delinsGCTGT	NP_054706.1:n.1353-19_1353-15delinsGCTGT
XM_005270142.1:c.1356-19_1356-15delinsGCTGT	XP_005270199.1:n.1356-19_1356-15delinsGCTGT
XM_005270143.1:c.1356-19_1356-15delinsGCTGT	XP_005270200.1:n.1356-19_1356-15delinsGCTGT
NM_003373.4:c.1353-19_1353-15delinsGCTGT	NP_003364.1:n.1353-19_1353-15delinsGCTGT
NM_014000.3:c.1353-19_1353-15delinsGCTGT MANE Select	NP_054706.1:n.1353-19_1353-15delinsGCTGT