Canonical Allele Identifier: CA1919908939

Gene: VCL

Linked Data

• dbSNP Id: rs1840372125

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74119565_74119568dup , CM000672.2:g.74119565_74119568dup	GRCh38
NC_000010.10:g.75879323_75879326dup , CM000672.1:g.75879323_75879326dup	GRCh37
NC_000010.9:g.75549329_75549332dup	NCBI36
NG_008868.1:g.126452_126455dup , LRG_383:g.126452_126455dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.*1396_*1399dup MANE Select	ENSP00000211998.5:n.*1396_*1399dup
ENST00000211998.8:c.*1396_*1399dup	ENSP00000211998.4:n.*1396_*1399dup
ENST00000372755.7:c.*1396_*1399dup	ENSP00000361841.3:n.*1396_*1399dup
ENST00000436396.1:c.3817_3820dup	ENSP00000415489.1:n.3817_3820dup
ENST00000623461.3:n.7400_7403dup
NM_003373.3:c.*1396_*1399dup	NP_003364.1:n.*1396_*1399dup
NM_014000.2:c.*1396_*1399dup , LRG_383t1:c.*1396_*1399dup	NP_054706.1:n.*1396_*1399dup
XM_005270142.1:c.*1396_*1399dup	XP_005270199.1:n.*1396_*1399dup
XM_005270143.1:c.*1396_*1399dup	XP_005270200.1:n.*1396_*1399dup
NM_003373.4:c.*1396_*1399dup	NP_003364.1:n.*1396_*1399dup
NM_014000.3:c.*1396_*1399dup MANE Select	NP_054706.1:n.*1396_*1399dup