Canonical Allele Identifier: CA377266203

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75830732G>T (hg19) ; chr10:g.74070974G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74070974G>T , CM000672.2:g.74070974G>T	GRCh38
NC_000010.10:g.75830732G>T , CM000672.1:g.75830732G>T	GRCh37
NC_000010.9:g.75500738G>T	NCBI36
NG_008868.1:g.77861G>T , LRG_383:g.77861G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.391-1G>T MANE Select	ENSP00000211998.5:n.391-1G>T
ENST00000211998.8:c.391-1G>T	ENSP00000211998.4:n.391-1G>T
ENST00000372755.7:c.391-1G>T	ENSP00000361841.3:n.391-1G>T
ENST00000478896.2:n.331+27821G>T
ENST00000623461.3:n.349-1G>T
ENST00000624354.3:c.*146-1G>T	ENSP00000485551.1:n.*146-1G>T
NM_003373.3:c.391-1G>T	NP_003364.1:n.391-1G>T
NM_014000.2:c.391-1G>T , LRG_383t1:c.391-1G>T	NP_054706.1:n.391-1G>T
XM_005270142.1:c.391-1G>T	XP_005270199.1:n.391-1G>T
XM_005270143.1:c.391-1G>T	XP_005270200.1:n.391-1G>T
NM_003373.4:c.391-1G>T	NP_003364.1:n.391-1G>T
NM_014000.3:c.391-1G>T MANE Select	NP_054706.1:n.391-1G>T