Canonical Allele Identifier: CA2537733088
Gene: VCL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74119476T>C , CM000672.2:g.74119476T>C GRCh38
NC_000010.10:g.75879234T>C , CM000672.1:g.75879234T>C GRCh37
NC_000010.9:g.75549240T>C NCBI36
NG_008868.1:g.126363T>C , LRG_383:g.126363T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000211998.10:c.*1307T>C MANE Select ENSP00000211998.5:n.*1307T>C
ENST00000211998.8:c.*1307T>C ENSP00000211998.4:n.*1307T>C
ENST00000372755.7:c.*1307T>C ENSP00000361841.3:n.*1307T>C
ENST00000436396.1:c.3728T>C ENSP00000415489.1:n.3728T>C
ENST00000623461.3:n.7311T>C
NM_003373.3:c.*1307T>C NP_003364.1:n.*1307T>C
NM_014000.2:c.*1307T>C , LRG_383t1:c.*1307T>C NP_054706.1:n.*1307T>C
XM_005270142.1:c.*1307T>C XP_005270199.1:n.*1307T>C
XM_005270143.1:c.*1307T>C XP_005270200.1:n.*1307T>C
NM_003373.4:c.*1307T>C NP_003364.1:n.*1307T>C
NM_014000.3:c.*1307T>C MANE Select NP_054706.1:n.*1307T>C