Canonical Allele Identifier: CA470165629

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75871816C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74112058C>A , CM000672.2:g.74112058C>A	GRCh38
NC_000010.10:g.75871816C>A , CM000672.1:g.75871816C>A	GRCh37
NC_000010.9:g.75541822C>A	NCBI36
NG_008868.1:g.118945C>A , LRG_383:g.118945C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.2895C>A MANE Select	ENSP00000211998.5:p.Pro965=
ENST00000211998.8:c.2895C>A	ENSP00000211998.4:p.Pro965=
ENST00000372755.7:c.2746-2126C>A	ENSP00000361841.3:n.2746-2126C>A
ENST00000436396.1:c.1911C>A	ENSP00000415489.1:p.Pro637=
ENST00000623461.3:n.5549-2126C>A
ENST00000624354.3:c.*2650C>A	ENSP00000485551.1:n.*2650C>A
NM_003373.3:c.2746-2126C>A	NP_003364.1:n.2746-2126C>A
NM_014000.2:c.2895C>A , LRG_383t1:c.2895C>A	NP_054706.1:p.Pro965=
XM_005270142.1:c.2898C>A	XP_005270199.1:p.Pro966=
XM_005270143.1:c.2749-2126C>A	XP_005270200.1:n.2749-2126C>A
NM_003373.4:c.2746-2126C>A	NP_003364.1:n.2746-2126C>A
NM_014000.3:c.2895C>A MANE Select	NP_054706.1:p.Pro965=