Canonical Allele Identifier: CA1919908957

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74119600_74119601delinsAT , CM000672.2:g.74119600_74119601delinsAT	GRCh38
NC_000010.10:g.75879358_75879359delinsAT , CM000672.1:g.75879358_75879359delinsAT	GRCh37
NC_000010.9:g.75549364_75549365delinsAT	NCBI36
NG_008868.1:g.126487_126488delinsAT , LRG_383:g.126487_126488delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.*1431_*1432delinsAT MANE Select	ENSP00000211998.5:n.*1431_*1432delinsAT
ENST00000211998.8:c.*1431_*1432delinsAT	ENSP00000211998.4:n.*1431_*1432delinsAT
ENST00000372755.7:c.*1431_*1432delinsAT	ENSP00000361841.3:n.*1431_*1432delinsAT
ENST00000436396.1:c.3852_3853delinsAT	ENSP00000415489.1:n.3852_3853delinsAT
ENST00000623461.3:n.7435_7436delinsAT
NM_003373.3:c.*1431_*1432delinsAT	NP_003364.1:n.*1431_*1432delinsAT
NM_014000.2:c.*1431_*1432delinsAT , LRG_383t1:c.*1431_*1432delinsAT	NP_054706.1:n.*1431_*1432delinsAT
XM_005270142.1:c.*1431_*1432delinsAT	XP_005270199.1:n.*1431_*1432delinsAT
XM_005270143.1:c.*1431_*1432delinsAT	XP_005270200.1:n.*1431_*1432delinsAT
NM_003373.4:c.*1431_*1432delinsAT	NP_003364.1:n.*1431_*1432delinsAT
NM_014000.3:c.*1431_*1432delinsAT MANE Select	NP_054706.1:n.*1431_*1432delinsAT