Canonical Allele Identifier: CA594393669

Gene: VCL

Linked Data

• dbSNP Id: rs1049552680
• gnomAD v2: 10-75830851-A-T
• gnomAD v4: 10-74071093-A-T
• MyVariant Identifiers: chr10:g.75830851A>T (hg19) ; chr10:g.74071093A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071093A>T , CM000672.2:g.74071093A>T	GRCh38
NC_000010.10:g.75830851A>T , CM000672.1:g.75830851A>T	GRCh37
NC_000010.9:g.75500857A>T	NCBI36
NG_008868.1:g.77980A>T , LRG_383:g.77980A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.499+10A>T MANE Select	ENSP00000211998.5:n.499+10A>T
ENST00000211998.8:c.499+10A>T	ENSP00000211998.4:n.499+10A>T
ENST00000372755.7:c.499+10A>T	ENSP00000361841.3:n.499+10A>T
ENST00000478896.2:n.331+27940A>T
ENST00000623461.3:n.457+10A>T
ENST00000624354.3:c.*254+10A>T	ENSP00000485551.1:n.*254+10A>T
NM_003373.3:c.499+10A>T	NP_003364.1:n.499+10A>T
NM_014000.2:c.499+10A>T , LRG_383t1:c.499+10A>T	NP_054706.1:n.499+10A>T
XM_005270142.1:c.499+10A>T	XP_005270199.1:n.499+10A>T
XM_005270143.1:c.499+10A>T	XP_005270200.1:n.499+10A>T
NM_003373.4:c.499+10A>T	NP_003364.1:n.499+10A>T
NM_014000.3:c.499+10A>T MANE Select	NP_054706.1:n.499+10A>T