Canonical Allele Identifier: CA2574585364

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071144_74071145insG , CM000672.2:g.74071144_74071145insG	GRCh38
NC_000010.10:g.75830902_75830903insG , CM000672.1:g.75830902_75830903insG	GRCh37
NC_000010.9:g.75500908_75500909insG	NCBI36
NG_008868.1:g.78031_78032insG , LRG_383:g.78031_78032insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.499+61_499+62insG MANE Select	ENSP00000211998.5:n.499+61_499+62insG
ENST00000211998.8:c.499+61_499+62insG	ENSP00000211998.4:n.499+61_499+62insG
ENST00000372755.7:c.499+61_499+62insG	ENSP00000361841.3:n.499+61_499+62insG
ENST00000478896.2:n.331+27991_331+27992insG
ENST00000623461.3:n.457+61_457+62insG
ENST00000624354.3:c.*254+61_*254+62insG	ENSP00000485551.1:n.*254+61_*254+62insG
NM_003373.3:c.499+61_499+62insG	NP_003364.1:n.499+61_499+62insG
NM_014000.2:c.499+61_499+62insG , LRG_383t1:c.499+61_499+62insG	NP_054706.1:n.499+61_499+62insG
XM_005270142.1:c.499+61_499+62insG	XP_005270199.1:n.499+61_499+62insG
XM_005270143.1:c.499+61_499+62insG	XP_005270200.1:n.499+61_499+62insG
NM_003373.4:c.499+61_499+62insG	NP_003364.1:n.499+61_499+62insG
NM_014000.3:c.499+61_499+62insG MANE Select	NP_054706.1:n.499+61_499+62insG