Canonical Allele Identifier: CA814712659
Gene: VCAN HGNC NCBI
VCAN-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs186066542
gnomAD v3: 5-83515566-A-G
gnomAD v4: 5-83515566-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.83515566A>G , CM000667.2:g.83515566A>G GRCh38
NC_000005.9:g.82811385A>G , CM000667.1:g.82811385A>G GRCh37
NC_000005.8:g.82847141A>G NCBI36
NG_012682.1:g.48856A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265077.8:c.1042+3170A>G (VCAN) MANE Select ENSP00000265077.3:n.1042+3170A>G
ENST00000265077.7:c.1042+3170A>G (VCAN) ENSP00000265077.3:n.1042+3170A>G
ENST00000342785.8:c.1042+3170A>G (VCAN) ENSP00000342768.4:n.1042+3170A>G
ENST00000343200.9:c.1042+3170A>G (VCAN) ENSP00000340062.5:n.1042+3170A>G
ENST00000502527.2:c.1042+3170A>G (VCAN) ENSP00000421362.2:n.1042+3170A>G
ENST00000512590.6:c.898+3170A>G (VCAN) ENSP00000425959.2:n.898+3170A>G
ENST00000513960.5:c.1042+3170A>G (VCAN) ENSP00000426251.1:n.1042+3170A>G
ENST00000515397.1:n.295+3170A>G (VCAN)
NM_001126336.2:c.1042+3170A>G (VCAN) NP_001119808.1:n.1042+3170A>G
NM_001164097.1:c.1042+3170A>G (VCAN) NP_001157569.1:n.1042+3170A>G
NM_001164098.1:c.1042+3170A>G (VCAN) NP_001157570.1:n.1042+3170A>G
NM_004385.4:c.1042+3170A>G (VCAN) NP_004376.2:n.1042+3170A>G
XM_011543776.1:c.454-1910T>C (VCAN-AS1) XP_011542078.1:n.454-1910T>C
XM_011543777.1:c.445-1910T>C (VCAN-AS1) XP_011542079.1:n.445-1910T>C
XM_011543778.1:c.454-1910T>C (VCAN-AS1) XP_011542080.1:n.454-1910T>C
XM_011543779.1:c.482-1910T>C (VCAN-AS1) XP_011542081.1:n.482-1910T>C
XM_011543780.1:c.250-1910T>C (VCAN-AS1) XP_011542082.1:n.250-1910T>C
XM_011543781.1:c.454-5646T>C (VCAN-AS1) XP_011542083.1:n.454-5646T>C
XM_011543782.1:c.320-1910T>C (VCAN-AS1) XP_011542084.1:n.320-1910T>C
XR_948512.1:n.839-1910T>C (VCAN-AS1)
XR_948517.1:n.181-1910T>C (VCAN-AS1)
NM_004385.5:c.1042+3170A>G (VCAN) MANE Select NP_004376.2:n.1042+3170A>G
NM_001126336.3:c.1042+3170A>G (VCAN) NP_001119808.1:n.1042+3170A>G
NM_001164097.2:c.1042+3170A>G (VCAN) NP_001157569.1:n.1042+3170A>G
NM_001164098.2:c.1042+3170A>G (VCAN) NP_001157570.1:n.1042+3170A>G