Canonical Allele Identifier: CA2609728635

Gene: VCL

Linked Data

• gnomAD v4: 10-74101121-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74101121A>G , CM000672.2:g.74101121A>G	GRCh38
NC_000010.10:g.75860879A>G , CM000672.1:g.75860879A>G	GRCh37
NC_000010.9:g.75530885A>G	NCBI36
NG_008868.1:g.108008A>G , LRG_383:g.108008A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2022+24A>G MANE Select	ENSP00000211998.5:n.2022+24A>G
ENST00000211998.8:c.2022+24A>G	ENSP00000211998.4:n.2022+24A>G
ENST00000372755.7:c.2022+24A>G	ENSP00000361841.3:n.2022+24A>G
ENST00000436396.1:c.1038+24A>G	ENSP00000415489.1:n.1038+24A>G
ENST00000478896.2:n.375+24A>G
ENST00000623461.3:n.4825+24A>G
ENST00000624354.3:c.*1777+24A>G	ENSP00000485551.1:n.*1777+24A>G
NM_003373.3:c.2022+24A>G	NP_003364.1:n.2022+24A>G
NM_014000.2:c.2022+24A>G , LRG_383t1:c.2022+24A>G	NP_054706.1:n.2022+24A>G
XM_005270142.1:c.2025+24A>G	XP_005270199.1:n.2025+24A>G
XM_005270143.1:c.2025+24A>G	XP_005270200.1:n.2025+24A>G
NM_003373.4:c.2022+24A>G	NP_003364.1:n.2022+24A>G
NM_014000.3:c.2022+24A>G MANE Select	NP_054706.1:n.2022+24A>G