Canonical Allele Identifier: CA15641372

Gene: VCL

Linked Data

• dbSNP Id: rs143333136
• gnomAD v2: 10-75830995-T-G
• gnomAD v3: 10-74071237-T-G
• gnomAD v4: 10-74071237-T-G
• MyVariant Identifiers: chr10:g.75830995T>G (hg19) ; chr10:g.74071237T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071237T>G , CM000672.2:g.74071237T>G	GRCh38
NC_000010.10:g.75830995T>G , CM000672.1:g.75830995T>G	GRCh37
NC_000010.9:g.75501001T>G	NCBI36
NG_008868.1:g.78124T>G , LRG_383:g.78124T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.499+154T>G MANE Select	ENSP00000211998.5:n.499+154T>G
ENST00000211998.8:c.499+154T>G	ENSP00000211998.4:n.499+154T>G
ENST00000372755.7:c.499+154T>G	ENSP00000361841.3:n.499+154T>G
ENST00000478896.2:n.331+28084T>G
ENST00000623461.3:n.457+154T>G
ENST00000624354.3:c.*254+154T>G	ENSP00000485551.1:n.*254+154T>G
NM_003373.3:c.499+154T>G	NP_003364.1:n.499+154T>G
NM_014000.2:c.499+154T>G , LRG_383t1:c.499+154T>G	NP_054706.1:n.499+154T>G
XM_005270142.1:c.499+154T>G	XP_005270199.1:n.499+154T>G
XM_005270143.1:c.499+154T>G	XP_005270200.1:n.499+154T>G
NM_003373.4:c.499+154T>G	NP_003364.1:n.499+154T>G
NM_014000.3:c.499+154T>G MANE Select	NP_054706.1:n.499+154T>G