Canonical Allele Identifier: CA2574585553

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74101110T>C , CM000672.2:g.74101110T>C	GRCh38
NC_000010.10:g.75860868T>C , CM000672.1:g.75860868T>C	GRCh37
NC_000010.9:g.75530874T>C	NCBI36
NG_008868.1:g.107997T>C , LRG_383:g.107997T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2022+13T>C MANE Select	ENSP00000211998.5:n.2022+13T>C
ENST00000211998.8:c.2022+13T>C	ENSP00000211998.4:n.2022+13T>C
ENST00000372755.7:c.2022+13T>C	ENSP00000361841.3:n.2022+13T>C
ENST00000436396.1:c.1038+13T>C	ENSP00000415489.1:n.1038+13T>C
ENST00000478896.2:n.375+13T>C
ENST00000623461.3:n.4825+13T>C
ENST00000624354.3:c.*1777+13T>C	ENSP00000485551.1:n.*1777+13T>C
NM_003373.3:c.2022+13T>C	NP_003364.1:n.2022+13T>C
NM_014000.2:c.2022+13T>C , LRG_383t1:c.2022+13T>C	NP_054706.1:n.2022+13T>C
XM_005270142.1:c.2025+13T>C	XP_005270199.1:n.2025+13T>C
XM_005270143.1:c.2025+13T>C	XP_005270200.1:n.2025+13T>C
NM_003373.4:c.2022+13T>C	NP_003364.1:n.2022+13T>C
NM_014000.3:c.2022+13T>C MANE Select	NP_054706.1:n.2022+13T>C