Canonical Allele Identifier: CA2609718339

Gene: VCL

Linked Data

• gnomAD v4: 10-74082382-TCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74082383_74082385del , CM000672.2:g.74082383_74082385del	GRCh38
NC_000010.10:g.75842141_75842143del , CM000672.1:g.75842141_75842143del	GRCh37
NC_000010.9:g.75512147_75512149del	NCBI36
NG_008868.1:g.89270_89272del , LRG_383:g.89270_89272del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.784-71_784-69del MANE Select	ENSP00000211998.5:n.784-71_784-69del
ENST00000211998.8:c.784-71_784-69del	ENSP00000211998.4:n.784-71_784-69del
ENST00000372755.7:c.784-71_784-69del	ENSP00000361841.3:n.784-71_784-69del
ENST00000478896.2:n.332-18671_332-18669del
ENST00000623461.3:n.3587-71_3587-69del
ENST00000624354.3:c.*539-71_*539-69del	ENSP00000485551.1:n.*539-71_*539-69del
NM_003373.3:c.784-71_784-69del	NP_003364.1:n.784-71_784-69del
NM_014000.2:c.784-71_784-69del , LRG_383t1:c.784-71_784-69del	NP_054706.1:n.784-71_784-69del
XM_005270142.1:c.784-68_784-66del	XP_005270199.1:n.784-68_784-66del
XM_005270143.1:c.784-68_784-66del	XP_005270200.1:n.784-68_784-66del
XR_001747501.1:n.90-4658_90-4656del
NM_003373.4:c.784-71_784-69del	NP_003364.1:n.784-71_784-69del
NM_014000.3:c.784-71_784-69del MANE Select	NP_054706.1:n.784-71_784-69del