Canonical Allele Identifier: CA668310753

Gene: VCL

Linked Data

• dbSNP Id: rs1442100557
• gnomAD v3: 10-74112163-GT-G
• gnomAD v4: 10-74112163-GT-G
• MyVariant Identifiers: chr10:g.75871922del (hg19) ; chr10:g.74112164del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74112164del , CM000672.2:g.74112164del	GRCh38
NC_000010.10:g.75871922del , CM000672.1:g.75871922del	GRCh37
NC_000010.9:g.75541928del	NCBI36
NG_008868.1:g.119051del , LRG_383:g.119051del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2949+52del MANE Select	ENSP00000211998.5:n.2949+52del
ENST00000211998.8:c.2949+52del	ENSP00000211998.4:n.2949+52del
ENST00000372755.7:c.2746-2020del	ENSP00000361841.3:n.2746-2020del
ENST00000436396.1:c.1965+52del	ENSP00000415489.1:n.1965+52del
ENST00000623461.3:n.5549-2020del
ENST00000624354.3:c.*2704+52del	ENSP00000485551.1:n.*2704+52del
NM_003373.3:c.2746-2020del	NP_003364.1:n.2746-2020del
NM_014000.2:c.2949+52del , LRG_383t1:c.2949+52del	NP_054706.1:n.2949+52del
XM_005270142.1:c.2952+52del	XP_005270199.1:n.2952+52del
XM_005270143.1:c.2749-2020del	XP_005270200.1:n.2749-2020del
NM_003373.4:c.2746-2020del	NP_003364.1:n.2746-2020del
NM_014000.3:c.2949+52del MANE Select	NP_054706.1:n.2949+52del