Canonical Allele Identifier: CA15367564
Gene: VCAN HGNC NCBI
VCAN-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs173686

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.83515681A>G , CM000667.2:g.83515681A>G GRCh38
NC_000005.9:g.82811500A>G , CM000667.1:g.82811500A>G GRCh37
NC_000005.8:g.82847256A>G NCBI36
NG_012682.1:g.48971A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000265077.8:c.1042+3285A>G (VCAN) MANE Select ENSP00000265077.3:p.=
ENST00000265077.7:c.1042+3285A>G ENSP00000265077.3:p.=
ENST00000342785.8:c.1042+3285A>G ENSP00000342768.4:p.=
ENST00000343200.9:c.1042+3285A>G ENSP00000340062.5:p.=
ENST00000502527.2:c.1042+3285A>G ENSP00000421362.2:p.=
ENST00000512590.6:c.898+3285A>G ENSP00000425959.2:p.=
ENST00000513960.5:c.1042+3285A>G ENSP00000426251.1:p.=
ENST00000515397.1:n.295+3285A>G
NM_001126336.2:c.1042+3285A>G (VCAN) NP_001119808.1:p.=
NM_001164097.1:c.1042+3285A>G (VCAN) NP_001157569.1:p.=
NM_001164098.1:c.1042+3285A>G (VCAN) NP_001157570.1:p.=
NM_004385.4:c.1042+3285A>G (VCAN) NP_004376.2:p.=
XM_011543776.1:c.454-2025T>C (VCAN-AS1) XP_011542078.1:p.=
XM_011543777.1:c.445-2025T>C (VCAN-AS1) XP_011542079.1:p.=
XM_011543778.1:c.454-2025T>C (VCAN-AS1) XP_011542080.1:p.=
XM_011543779.1:c.482-2025T>C (VCAN-AS1) XP_011542081.1:p.=
XM_011543780.1:c.250-2025T>C (VCAN-AS1) XP_011542082.1:p.=
XM_011543781.1:c.454-5761T>C (VCAN-AS1) XP_011542083.1:p.=
XM_011543782.1:c.320-2025T>C (VCAN-AS1) XP_011542084.1:p.=
XR_948512.1:n.839-2025T>C (VCAN-AS1)
XR_948517.1:n.181-2025T>C (VCAN-AS1)
NM_004385.5:c.1042+3285A>G (VCAN) MANE Select NP_004376.2:p.=
NM_001126336.3:c.1042+3285A>G (VCAN) NP_001119808.1:p.=
NM_001164097.2:c.1042+3285A>G (VCAN) NP_001157569.1:p.=
NM_001164098.2:c.1042+3285A>G (VCAN) NP_001157570.1:p.=