Canonical Allele Identifier: CA5563144

Gene: VCL

Linked Data

• dbSNP Id: rs760897596
• ExAC: 10:75860885 TTC / T
• gnomAD v2: 10-75860885-TTC-T
• gnomAD v4: 10-74101127-TTC-T
• MyVariant Identifiers: chr10:g.75860886_75860887del (hg19) ; chr10:g.74101128_74101129del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74101128_74101129del , CM000672.2:g.74101128_74101129del	GRCh38
NC_000010.10:g.75860886_75860887del , CM000672.1:g.75860886_75860887del	GRCh37
NC_000010.9:g.75530892_75530893del	NCBI36
NG_008868.1:g.108015_108016del , LRG_383:g.108015_108016del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2022+31_2022+32del MANE Select	ENSP00000211998.5:n.2022+31_2022+32del
ENST00000211998.8:c.2022+31_2022+32del	ENSP00000211998.4:n.2022+31_2022+32del
ENST00000372755.7:c.2022+31_2022+32del	ENSP00000361841.3:n.2022+31_2022+32del
ENST00000436396.1:c.1038+31_1038+32del	ENSP00000415489.1:n.1038+31_1038+32del
ENST00000478896.2:n.375+31_375+32del
ENST00000623461.3:n.4825+31_4825+32del
ENST00000624354.3:c.*1777+31_*1777+32del	ENSP00000485551.1:n.*1777+31_*1777+32del
NM_003373.3:c.2022+31_2022+32del	NP_003364.1:n.2022+31_2022+32del
NM_014000.2:c.2022+31_2022+32del , LRG_383t1:c.2022+31_2022+32del	NP_054706.1:n.2022+31_2022+32del
XM_005270142.1:c.2025+31_2025+32del	XP_005270199.1:n.2025+31_2025+32del
XM_005270143.1:c.2025+31_2025+32del	XP_005270200.1:n.2025+31_2025+32del
NM_003373.4:c.2022+31_2022+32del	NP_003364.1:n.2022+31_2022+32del
NM_014000.3:c.2022+31_2022+32del MANE Select	NP_054706.1:n.2022+31_2022+32del