Canonical Allele Identifier: CA668315436

Gene: VCL

Linked Data

• dbSNP Id: rs1159655540
• MyVariant Identifiers: chr10:g.75879127T>G (hg19) ; chr10:g.74119369T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74119369T>G , CM000672.2:g.74119369T>G	GRCh38
NC_000010.10:g.75879127T>G , CM000672.1:g.75879127T>G	GRCh37
NC_000010.9:g.75549133T>G	NCBI36
NG_008868.1:g.126256T>G , LRG_383:g.126256T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.*1200T>G MANE Select	ENSP00000211998.5:n.*1200T>G
ENST00000211998.8:c.*1200T>G	ENSP00000211998.4:n.*1200T>G
ENST00000372755.7:c.*1200T>G	ENSP00000361841.3:n.*1200T>G
ENST00000436396.1:c.3621T>G	ENSP00000415489.1:n.3621T>G
ENST00000623461.3:n.7204T>G
NM_003373.3:c.*1200T>G	NP_003364.1:n.*1200T>G
NM_014000.2:c.*1200T>G , LRG_383t1:c.*1200T>G	NP_054706.1:n.*1200T>G
XM_005270142.1:c.*1200T>G	XP_005270199.1:n.*1200T>G
XM_005270143.1:c.*1200T>G	XP_005270200.1:n.*1200T>G
NM_003373.4:c.*1200T>G	NP_003364.1:n.*1200T>G
NM_014000.3:c.*1200T>G MANE Select	NP_054706.1:n.*1200T>G