Canonical Allele Identifier: CA658780791

Gene: VCL

Linked Data

• dbSNP Id: rs1841657077
• gnomAD v4: 10-74071088-G-C
• PubMed: PMID:25363768

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071088G>C , CM000672.2:g.74071088G>C	GRCh38
NC_000010.10:g.75830846G>C , CM000672.1:g.75830846G>C	GRCh37
NC_000010.9:g.75500852G>C	NCBI36
NG_008868.1:g.77975G>C , LRG_383:g.77975G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.499+5G>C MANE Select	ENSP00000211998.5:n.499+5G>C
ENST00000211998.8:c.499+5G>C	ENSP00000211998.4:n.499+5G>C
ENST00000372755.7:c.499+5G>C	ENSP00000361841.3:n.499+5G>C
ENST00000478896.2:n.331+27935G>C
ENST00000623461.3:n.457+5G>C
ENST00000624354.3:c.*254+5G>C	ENSP00000485551.1:n.*254+5G>C
NM_003373.3:c.499+5G>C	NP_003364.1:n.499+5G>C
NM_014000.2:c.499+5G>C , LRG_383t1:c.499+5G>C	NP_054706.1:n.499+5G>C
XM_005270142.1:c.499+5G>C	XP_005270199.1:n.499+5G>C
XM_005270143.1:c.499+5G>C	XP_005270200.1:n.499+5G>C
NM_003373.4:c.499+5G>C	NP_003364.1:n.499+5G>C
NM_014000.3:c.499+5G>C MANE Select	NP_054706.1:n.499+5G>C