Canonical Allele Identifier: CA2524874178
Gene: VCL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74101115_74101116insTTTTATTATGCG , CM000672.2:g.74101115_74101116insTTTTATTATGCG GRCh38
NC_000010.10:g.75860873_75860874insTTTTATTATGCG , CM000672.1:g.75860873_75860874insTTTTATTATGCG GRCh37
NC_000010.9:g.75530879_75530880insTTTTATTATGCG NCBI36
NG_008868.1:g.108002_108003insTTTTATTATGCG , LRG_383:g.108002_108003insTTTTATTATGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000211998.10:c.2022+18_2022+19insTTTTATTATGCG MANE Select ENSP00000211998.5:n.2022+18_2022+19insTTTTATTATGCG
ENST00000211998.8:c.2022+18_2022+19insTTTTATTATGCG ENSP00000211998.4:n.2022+18_2022+19insTTTTATTATGCG
ENST00000372755.7:c.2022+18_2022+19insTTTTATTATGCG ENSP00000361841.3:n.2022+18_2022+19insTTTTATTATGCG
ENST00000436396.1:c.1038+18_1038+19insTTTTATTATGCG ENSP00000415489.1:n.1038+18_1038+19insTTTTATTATGCG
ENST00000478896.2:n.375+18_375+19insTTTTATTATGCG
ENST00000623461.3:n.4825+18_4825+19insTTTTATTATGCG
ENST00000624354.3:c.*1777+18_*1777+19insTTTTATTATGCG ENSP00000485551.1:n.*1777+18_*1777+19insTTTTATTATGCG
NM_003373.3:c.2022+18_2022+19insTTTTATTATGCG NP_003364.1:n.2022+18_2022+19insTTTTATTATGCG
NM_014000.2:c.2022+18_2022+19insTTTTATTATGCG , LRG_383t1:c.2022+18_2022+19insTTTTATTATGCG NP_054706.1:n.2022+18_2022+19insTTTTATTATGCG
XM_005270142.1:c.2025+18_2025+19insTTTTATTATGCG XP_005270199.1:n.2025+18_2025+19insTTTTATTATGCG
XM_005270143.1:c.2025+18_2025+19insTTTTATTATGCG XP_005270200.1:n.2025+18_2025+19insTTTTATTATGCG
NM_003373.4:c.2022+18_2022+19insTTTTATTATGCG NP_003364.1:n.2022+18_2022+19insTTTTATTATGCG
NM_014000.3:c.2022+18_2022+19insTTTTATTATGCG MANE Select NP_054706.1:n.2022+18_2022+19insTTTTATTATGCG