Canonical Allele Identifier: CA2501991846

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74101126_74101133del , CM000672.2:g.74101126_74101133del	GRCh38
NC_000010.10:g.75860884_75860891del , CM000672.1:g.75860884_75860891del	GRCh37
NC_000010.9:g.75530890_75530897del	NCBI36
NG_008868.1:g.108013_108020del , LRG_383:g.108013_108020del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2022+29_2022+36del MANE Select	ENSP00000211998.5:n.2022+29_2022+36del
ENST00000211998.8:c.2022+29_2022+36del	ENSP00000211998.4:n.2022+29_2022+36del
ENST00000372755.7:c.2022+29_2022+36del	ENSP00000361841.3:n.2022+29_2022+36del
ENST00000436396.1:c.1038+29_1038+36del	ENSP00000415489.1:n.1038+29_1038+36del
ENST00000478896.2:n.375+29_375+36del
ENST00000623461.3:n.4825+29_4825+36del
ENST00000624354.3:c.*1777+29_*1777+36del	ENSP00000485551.1:n.*1777+29_*1777+36del
NM_003373.3:c.2022+29_2022+36del	NP_003364.1:n.2022+29_2022+36del
NM_014000.2:c.2022+29_2022+36del , LRG_383t1:c.2022+29_2022+36del	NP_054706.1:n.2022+29_2022+36del
XM_005270142.1:c.2025+29_2025+36del	XP_005270199.1:n.2025+29_2025+36del
XM_005270143.1:c.2025+29_2025+36del	XP_005270200.1:n.2025+29_2025+36del
NM_003373.4:c.2022+29_2022+36del	NP_003364.1:n.2022+29_2022+36del
NM_014000.3:c.2022+29_2022+36del MANE Select	NP_054706.1:n.2022+29_2022+36del