Canonical Allele Identifier: CA2544302647

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74101119_74101120insCCA , CM000672.2:g.74101119_74101120insCCA	GRCh38
NC_000010.10:g.75860877_75860878insCCA , CM000672.1:g.75860877_75860878insCCA	GRCh37
NC_000010.9:g.75530883_75530884insCCA	NCBI36
NG_008868.1:g.108006_108007insCCA , LRG_383:g.108006_108007insCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2022+22_2022+23insCCA MANE Select	ENSP00000211998.5:n.2022+22_2022+23insCCA
ENST00000211998.8:c.2022+22_2022+23insCCA	ENSP00000211998.4:n.2022+22_2022+23insCCA
ENST00000372755.7:c.2022+22_2022+23insCCA	ENSP00000361841.3:n.2022+22_2022+23insCCA
ENST00000436396.1:c.1038+22_1038+23insCCA	ENSP00000415489.1:n.1038+22_1038+23insCCA
ENST00000478896.2:n.375+22_375+23insCCA
ENST00000623461.3:n.4825+22_4825+23insCCA
ENST00000624354.3:c.*1777+22_*1777+23insCCA	ENSP00000485551.1:n.*1777+22_*1777+23insCCA
NM_003373.3:c.2022+22_2022+23insCCA	NP_003364.1:n.2022+22_2022+23insCCA
NM_014000.2:c.2022+22_2022+23insCCA , LRG_383t1:c.2022+22_2022+23insCCA	NP_054706.1:n.2022+22_2022+23insCCA
XM_005270142.1:c.2025+22_2025+23insCCA	XP_005270199.1:n.2025+22_2025+23insCCA
XM_005270143.1:c.2025+22_2025+23insCCA	XP_005270200.1:n.2025+22_2025+23insCCA
NM_003373.4:c.2022+22_2022+23insCCA	NP_003364.1:n.2022+22_2022+23insCCA
NM_014000.3:c.2022+22_2022+23insCCA MANE Select	NP_054706.1:n.2022+22_2022+23insCCA