Canonical Allele Identifier: CA470165463

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75871723C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74111965C>G , CM000672.2:g.74111965C>G	GRCh38
NC_000010.10:g.75871723C>G , CM000672.1:g.75871723C>G	GRCh37
NC_000010.9:g.75541729C>G	NCBI36
NG_008868.1:g.118852C>G , LRG_383:g.118852C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.2802C>G MANE Select	ENSP00000211998.5:p.Ala934=
ENST00000211998.8:c.2802C>G	ENSP00000211998.4:p.Ala934=
ENST00000372755.7:c.2746-2219C>G	ENSP00000361841.3:n.2746-2219C>G
ENST00000436396.1:c.1818C>G	ENSP00000415489.1:p.Ala606=
ENST00000623461.3:n.5549-2219C>G
ENST00000624354.3:c.*2557C>G	ENSP00000485551.1:n.*2557C>G
NM_003373.3:c.2746-2219C>G	NP_003364.1:n.2746-2219C>G
NM_014000.2:c.2802C>G , LRG_383t1:c.2802C>G	NP_054706.1:p.Ala934=
XM_005270142.1:c.2805C>G	XP_005270199.1:p.Ala935=
XM_005270143.1:c.2749-2219C>G	XP_005270200.1:n.2749-2219C>G
NM_003373.4:c.2746-2219C>G	NP_003364.1:n.2746-2219C>G
NM_014000.3:c.2802C>G MANE Select	NP_054706.1:p.Ala934=