Canonical Allele Identifier: CA1919905842

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74112134_74112135delinsTG , CM000672.2:g.74112134_74112135delinsTG	GRCh38
NC_000010.10:g.75871892_75871893delinsTG , CM000672.1:g.75871892_75871893delinsTG	GRCh37
NC_000010.9:g.75541898_75541899delinsTG	NCBI36
NG_008868.1:g.119021_119022delinsTG , LRG_383:g.119021_119022delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2949+22_2949+23delinsTG MANE Select	ENSP00000211998.5:n.2949+22_2949+23delinsTG
ENST00000211998.8:c.2949+22_2949+23delinsTG	ENSP00000211998.4:n.2949+22_2949+23delinsTG
ENST00000372755.7:c.2746-2050_2746-2049delinsTG	ENSP00000361841.3:n.2746-2050_2746-2049delinsTG
ENST00000436396.1:c.1965+22_1965+23delinsTG	ENSP00000415489.1:n.1965+22_1965+23delinsTG
ENST00000623461.3:n.5549-2050_5549-2049delinsTG
ENST00000624354.3:c.*2704+22_*2704+23delinsTG	ENSP00000485551.1:n.*2704+22_*2704+23delinsTG
NM_003373.3:c.2746-2050_2746-2049delinsTG	NP_003364.1:n.2746-2050_2746-2049delinsTG
NM_014000.2:c.2949+22_2949+23delinsTG , LRG_383t1:c.2949+22_2949+23delinsTG	NP_054706.1:n.2949+22_2949+23delinsTG
XM_005270142.1:c.2952+22_2952+23delinsTG	XP_005270199.1:n.2952+22_2952+23delinsTG
XM_005270143.1:c.2749-2050_2749-2049delinsTG	XP_005270200.1:n.2749-2050_2749-2049delinsTG
NM_003373.4:c.2746-2050_2746-2049delinsTG	NP_003364.1:n.2746-2050_2746-2049delinsTG
NM_014000.3:c.2949+22_2949+23delinsTG MANE Select	NP_054706.1:n.2949+22_2949+23delinsTG