Canonical Allele Identifier: CA2505433850
Gene: VCL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74107168G>T , CM000672.2:g.74107168G>T GRCh38
NC_000010.10:g.75866926G>T , CM000672.1:g.75866926G>T GRCh37
NC_000010.9:g.75536932G>T NCBI36
NG_008868.1:g.114055G>T , LRG_383:g.114055G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000211998.10:c.2435-62G>T MANE Select ENSP00000211998.5:n.2435-62G>T
ENST00000211998.8:c.2435-62G>T ENSP00000211998.4:n.2435-62G>T
ENST00000372755.7:c.2435-62G>T ENSP00000361841.3:n.2435-62G>T
ENST00000436396.1:c.1451-62G>T ENSP00000415489.1:n.1451-62G>T
ENST00000472585.1:n.427-62G>T
ENST00000623461.3:n.5238-62G>T
ENST00000624354.3:c.*2190-62G>T ENSP00000485551.1:n.*2190-62G>T
NM_003373.3:c.2435-62G>T NP_003364.1:n.2435-62G>T
NM_014000.2:c.2435-62G>T , LRG_383t1:c.2435-62G>T NP_054706.1:n.2435-62G>T
XM_005270142.1:c.2438-62G>T XP_005270199.1:n.2438-62G>T
XM_005270143.1:c.2438-62G>T XP_005270200.1:n.2438-62G>T
NM_003373.4:c.2435-62G>T NP_003364.1:n.2435-62G>T
NM_014000.3:c.2435-62G>T MANE Select NP_054706.1:n.2435-62G>T