Canonical Allele Identifier: CA2543728186

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74101136_74101137insT , CM000672.2:g.74101136_74101137insT	GRCh38
NC_000010.10:g.75860894_75860895insT , CM000672.1:g.75860894_75860895insT	GRCh37
NC_000010.9:g.75530900_75530901insT	NCBI36
NG_008868.1:g.108023_108024insT , LRG_383:g.108023_108024insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2022+39_2022+40insT MANE Select	ENSP00000211998.5:n.2022+39_2022+40insT
ENST00000211998.8:c.2022+39_2022+40insT	ENSP00000211998.4:n.2022+39_2022+40insT
ENST00000372755.7:c.2022+39_2022+40insT	ENSP00000361841.3:n.2022+39_2022+40insT
ENST00000436396.1:c.1038+39_1038+40insT	ENSP00000415489.1:n.1038+39_1038+40insT
ENST00000478896.2:n.375+39_375+40insT
ENST00000623461.3:n.4825+39_4825+40insT
ENST00000624354.3:c.*1777+39_*1777+40insT	ENSP00000485551.1:n.*1777+39_*1777+40insT
NM_003373.3:c.2022+39_2022+40insT	NP_003364.1:n.2022+39_2022+40insT
NM_014000.2:c.2022+39_2022+40insT , LRG_383t1:c.2022+39_2022+40insT	NP_054706.1:n.2022+39_2022+40insT
XM_005270142.1:c.2025+39_2025+40insT	XP_005270199.1:n.2025+39_2025+40insT
XM_005270143.1:c.2025+39_2025+40insT	XP_005270200.1:n.2025+39_2025+40insT
NM_003373.4:c.2022+39_2022+40insT	NP_003364.1:n.2022+39_2022+40insT
NM_014000.3:c.2022+39_2022+40insT MANE Select	NP_054706.1:n.2022+39_2022+40insT