Canonical Allele Identifier: CA2842427063

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74111961del , CM000672.2:g.74111961del	GRCh38
NC_000010.10:g.75871719del , CM000672.1:g.75871719del	GRCh37
NC_000010.9:g.75541725del	NCBI36
NG_008868.1:g.118848del , LRG_383:g.118848del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2798del MANE Select	ENSP00000211998.5:p.Ala933GlyfsTer23
ENST00000211998.8:c.2798del	ENSP00000211998.4:p.Ala933GlyfsTer23
ENST00000372755.7:c.2746-2223del	ENSP00000361841.3:n.2746-2223del
ENST00000436396.1:c.1814del	ENSP00000415489.1:p.Ala605GlyfsTer23
ENST00000623461.3:n.5549-2223del
ENST00000624354.3:c.*2553del	ENSP00000485551.1:n.*2553del
NM_003373.3:c.2746-2223del	NP_003364.1:n.2746-2223del
NM_014000.2:c.2798del , LRG_383t1:c.2798del	NP_054706.1:p.Ala933GlyfsTer23
XM_005270142.1:c.2801del	XP_005270199.1:p.Ala934GlyfsTer23
XM_005270143.1:c.2749-2223del	XP_005270200.1:n.2749-2223del
NM_003373.4:c.2746-2223del	NP_003364.1:n.2746-2223del
NM_014000.3:c.2798del MANE Select	NP_054706.1:p.Ala933GlyfsTer23