Canonical Allele Identifier: CA1919897551

Gene: VCL

Linked Data

• dbSNP Id: rs1839690341
• gnomAD v4: 10-74082383-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74082383C>T , CM000672.2:g.74082383C>T	GRCh38
NC_000010.10:g.75842141C>T , CM000672.1:g.75842141C>T	GRCh37
NC_000010.9:g.75512147C>T	NCBI36
NG_008868.1:g.89270C>T , LRG_383:g.89270C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.784-71C>T MANE Select	ENSP00000211998.5:n.784-71C>T
ENST00000211998.8:c.784-71C>T	ENSP00000211998.4:n.784-71C>T
ENST00000372755.7:c.784-71C>T	ENSP00000361841.3:n.784-71C>T
ENST00000478896.2:n.332-18671C>T
ENST00000623461.3:n.3587-71C>T
ENST00000624354.3:c.*539-71C>T	ENSP00000485551.1:n.*539-71C>T
NM_003373.3:c.784-71C>T	NP_003364.1:n.784-71C>T
NM_014000.2:c.784-71C>T , LRG_383t1:c.784-71C>T	NP_054706.1:n.784-71C>T
XM_005270142.1:c.784-68C>T	XP_005270199.1:n.784-68C>T
XM_005270143.1:c.784-68C>T	XP_005270200.1:n.784-68C>T
XR_001747501.1:n.90-4656G>A
NM_003373.4:c.784-71C>T	NP_003364.1:n.784-71C>T
NM_014000.3:c.784-71C>T MANE Select	NP_054706.1:n.784-71C>T