Canonical Allele Identifier: CA2609715363

Gene: VCL

Linked Data

• gnomAD v4: 10-74070855-G-GAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74070857_74070858dup , CM000672.2:g.74070857_74070858dup	GRCh38
NC_000010.10:g.75830615_75830616dup , CM000672.1:g.75830615_75830616dup	GRCh37
NC_000010.9:g.75500621_75500622dup	NCBI36
NG_008868.1:g.77744_77745dup , LRG_383:g.77744_77745dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.390+37_390+38dup MANE Select	ENSP00000211998.5:n.390+37_390+38dup
ENST00000211998.8:c.390+37_390+38dup	ENSP00000211998.4:n.390+37_390+38dup
ENST00000372755.7:c.390+37_390+38dup	ENSP00000361841.3:n.390+37_390+38dup
ENST00000478896.2:n.331+27704_331+27705dup
ENST00000623461.3:n.348+37_348+38dup
ENST00000624354.3:c.*145+37_*145+38dup	ENSP00000485551.1:n.*145+37_*145+38dup
NM_003373.3:c.390+37_390+38dup	NP_003364.1:n.390+37_390+38dup
NM_014000.2:c.390+37_390+38dup , LRG_383t1:c.390+37_390+38dup	NP_054706.1:n.390+37_390+38dup
XM_005270142.1:c.390+37_390+38dup	XP_005270199.1:n.390+37_390+38dup
XM_005270143.1:c.390+37_390+38dup	XP_005270200.1:n.390+37_390+38dup
NM_003373.4:c.390+37_390+38dup	NP_003364.1:n.390+37_390+38dup
NM_014000.3:c.390+37_390+38dup MANE Select	NP_054706.1:n.390+37_390+38dup