Canonical Allele Identifier: CA209692512

Gene: VCL

Linked Data

• dbSNP Id: rs761167375
• gnomAD v4: 10-74071140-A-AGGAAAGG
• MyVariant Identifiers: chr10:g.75830898_75830899insGGAAAGG (hg19) ; chr10:g.74071140_74071141insGGAAAGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071142_74071148dup , CM000672.2:g.74071142_74071148dup	GRCh38
NC_000010.10:g.75830900_75830906dup , CM000672.1:g.75830900_75830906dup	GRCh37
NC_000010.9:g.75500906_75500912dup	NCBI36
NG_008868.1:g.78029_78035dup , LRG_383:g.78029_78035dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.499+59_499+65dup MANE Select	ENSP00000211998.5:n.499+59_499+65dup
ENST00000211998.8:c.499+59_499+65dup	ENSP00000211998.4:n.499+59_499+65dup
ENST00000372755.7:c.499+59_499+65dup	ENSP00000361841.3:n.499+59_499+65dup
ENST00000478896.2:n.331+27989_331+27995dup
ENST00000623461.3:n.457+59_457+65dup
ENST00000624354.3:c.*254+59_*254+65dup	ENSP00000485551.1:n.*254+59_*254+65dup
NM_003373.3:c.499+59_499+65dup	NP_003364.1:n.499+59_499+65dup
NM_014000.2:c.499+59_499+65dup , LRG_383t1:c.499+59_499+65dup	NP_054706.1:n.499+59_499+65dup
XM_005270142.1:c.499+59_499+65dup	XP_005270199.1:n.499+59_499+65dup
XM_005270143.1:c.499+59_499+65dup	XP_005270200.1:n.499+59_499+65dup
NM_003373.4:c.499+59_499+65dup	NP_003364.1:n.499+59_499+65dup
NM_014000.3:c.499+59_499+65dup MANE Select	NP_054706.1:n.499+59_499+65dup