Canonical Allele Identifier: CA1919897731

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74082548_74082552delinsACCCT , CM000672.2:g.74082548_74082552delinsACCCT	GRCh38
NC_000010.10:g.75842306_75842310delinsACCCT , CM000672.1:g.75842306_75842310delinsACCCT	GRCh37
NC_000010.9:g.75512312_75512316delinsACCCT	NCBI36
NG_008868.1:g.89435_89439delinsACCCT , LRG_383:g.89435_89439delinsACCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.874+4_874+8delinsACCCT MANE Select	ENSP00000211998.5:n.874+4_874+8delinsACCCT
ENST00000211998.8:c.874+4_874+8delinsACCCT	ENSP00000211998.4:n.874+4_874+8delinsACCCT
ENST00000372755.7:c.874+4_874+8delinsACCCT	ENSP00000361841.3:n.874+4_874+8delinsACCCT
ENST00000478896.2:n.332-18506_332-18502delinsACCCT
ENST00000623461.3:n.3677+4_3677+8delinsACCCT
ENST00000624354.3:c.*629+4_*629+8delinsACCCT	ENSP00000485551.1:n.*629+4_*629+8delinsACCCT
NM_003373.3:c.874+4_874+8delinsACCCT	NP_003364.1:n.874+4_874+8delinsACCCT
NM_014000.2:c.874+4_874+8delinsACCCT , LRG_383t1:c.874+4_874+8delinsACCCT	NP_054706.1:n.874+4_874+8delinsACCCT
XM_005270142.1:c.877+4_877+8delinsACCCT	XP_005270199.1:n.877+4_877+8delinsACCCT
XM_005270143.1:c.877+4_877+8delinsACCCT	XP_005270200.1:n.877+4_877+8delinsACCCT
XR_001747501.1:n.90-4825_90-4821delinsAGGGT
NM_003373.4:c.874+4_874+8delinsACCCT	NP_003364.1:n.874+4_874+8delinsACCCT
NM_014000.3:c.874+4_874+8delinsACCCT MANE Select	NP_054706.1:n.874+4_874+8delinsACCCT