Canonical Allele Identifier: CA377272311

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75848983A>C (hg19) ; chr10:g.74089225A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74089225A>C , CM000672.2:g.74089225A>C	GRCh38
NC_000010.10:g.75848983A>C , CM000672.1:g.75848983A>C	GRCh37
NC_000010.9:g.75518989A>C	NCBI36
NG_008868.1:g.96112A>C , LRG_383:g.96112A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.1052A>C MANE Select	ENSP00000211998.5:p.Gln351Pro
ENST00000211998.8:c.1052A>C	ENSP00000211998.4:p.Gln351Pro
ENST00000372755.7:c.1052A>C	ENSP00000361841.3:p.Gln351Pro
ENST00000436396.1:c.68A>C	ENSP00000415489.1:p.Gln23Pro
ENST00000478896.2:n.332-11829A>C
ENST00000623461.3:n.3855A>C
ENST00000624354.3:c.*807A>C	ENSP00000485551.1:n.*807A>C
NM_003373.3:c.1052A>C	NP_003364.1:p.Gln351Pro
NM_014000.2:c.1052A>C , LRG_383t1:c.1052A>C	NP_054706.1:p.Gln351Pro
XM_005270142.1:c.1055A>C	XP_005270199.1:p.Gln352Pro
XM_005270143.1:c.1055A>C	XP_005270200.1:p.Gln352Pro
XR_001747501.1:n.89+707T>G
NM_003373.4:c.1052A>C	NP_003364.1:p.Gln351Pro
NM_014000.3:c.1052A>C MANE Select	NP_054706.1:p.Gln351Pro