Canonical Allele Identifier: CA1919905840

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74112133_74112149delinsTTGGGGGCTGCTCCATA , CM000672.2:g.74112133_74112149delinsTTGGGGGCTGCTCCATA	GRCh38
NC_000010.10:g.75871891_75871907delinsTTGGGGGCTGCTCCATA , CM000672.1:g.75871891_75871907delinsTTGGGGGCTGCTCCATA	GRCh37
NC_000010.9:g.75541897_75541913delinsTTGGGGGCTGCTCCATA	NCBI36
NG_008868.1:g.119020_119036delinsTTGGGGGCTGCTCCATA , LRG_383:g.119020_119036delinsTTGGGGGCTGCTCCATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2949+21_2949+37delinsTTGGGGGCTGCTCCATA MANE Select	ENSP00000211998.5:n.2949+21_2949+37delinsTTGGGGGCTGCTCCATA
ENST00000211998.8:c.2949+21_2949+37delinsTTGGGGGCTGCTCCATA	ENSP00000211998.4:n.2949+21_2949+37delinsTTGGGGGCTGCTCCATA
ENST00000372755.7:c.2746-2051_2746-2035delinsTTGGGGGCTGCTCCATA	ENSP00000361841.3:n.2746-2051_2746-2035delinsTTGGGGGCTGCTCCAT...
ENST00000436396.1:c.1965+21_1965+37delinsTTGGGGGCTGCTCCATA	ENSP00000415489.1:n.1965+21_1965+37delinsTTGGGGGCTGCTCCATA
ENST00000623461.3:n.5549-2051_5549-2035delinsTTGGGGGCTGCTCCATA
ENST00000624354.3:c.*2704+21_*2704+37delinsTTGGGGGCTGCTCCATA	ENSP00000485551.1:n.*2704+21_*2704+37delinsTTGGGGGCTGCTCCATA
NM_003373.3:c.2746-2051_2746-2035delinsTTGGGGGCTGCTCCATA	NP_003364.1:n.2746-2051_2746-2035delinsTTGGGGGCTGCTCCATA
NM_014000.2:c.2949+21_2949+37delinsTTGGGGGCTGCTCCATA , LRG_383t1:c.2949+21_2949+37delinsTTGGGGGCTGCTCCATA	NP_054706.1:n.2949+21_2949+37delinsTTGGGGGCTGCTCCATA
XM_005270142.1:c.2952+21_2952+37delinsTTGGGGGCTGCTCCATA	XP_005270199.1:n.2952+21_2952+37delinsTTGGGGGCTGCTCCATA
XM_005270143.1:c.2749-2051_2749-2035delinsTTGGGGGCTGCTCCATA	XP_005270200.1:n.2749-2051_2749-2035delinsTTGGGGGCTGCTCCATA
NM_003373.4:c.2746-2051_2746-2035delinsTTGGGGGCTGCTCCATA	NP_003364.1:n.2746-2051_2746-2035delinsTTGGGGGCTGCTCCATA
NM_014000.3:c.2949+21_2949+37delinsTTGGGGGCTGCTCCATA MANE Select	NP_054706.1:n.2949+21_2949+37delinsTTGGGGGCTGCTCCATA