ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.83537005A>G , CM000667.2:g.83537005A>G | GRCh38 |
| NC_000005.9:g.82832824A>G , CM000667.1:g.82832824A>G | GRCh37 |
| NC_000005.8:g.82868580A>G | NCBI36 |
| NG_012682.1:g.70295A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265077.8:c.4004-2A>G (VCAN) MANE Select | ENSP00000265077.3:n.4004-2A>G | |
| ENST00000265077.7:c.4004-2A>G (VCAN) | ENSP00000265077.3:n.4004-2A>G | |
| ENST00000342785.8:c.4004-8532A>G (VCAN) | ENSP00000342768.4:n.4004-8532A>G | |
| ENST00000343200.9:c.1043-2A>G (VCAN) | ENSP00000340062.5:n.1043-2A>G | |
| ENST00000502527.2:c.1043-8532A>G (VCAN) | ENSP00000421362.2:n.1043-8532A>G | |
| ENST00000512590.6:c.3860-8532A>G (VCAN) | ENSP00000425959.2:n.3860-8532A>G | |
| ENST00000513016.5:n.1392A>G (VCAN) | ||
| ENST00000513960.5:c.1043-2A>G (VCAN) | ENSP00000426251.1:n.1043-2A>G | |
| ENST00000515397.1:n.296-2A>G (VCAN) | ||
| NM_001126336.2:c.1043-8532A>G (VCAN) | NP_001119808.1:n.1043-8532A>G | |
| NM_001164097.1:c.1043-2A>G (VCAN) | NP_001157569.1:n.1043-2A>G | |
| NM_001164098.1:c.4004-8532A>G (VCAN) | NP_001157570.1:n.4004-8532A>G | |
| NM_004385.4:c.4004-2A>G (VCAN) | NP_004376.2:n.4004-2A>G | |
| XM_011543776.1:c.161-2823T>C (VCAN-AS1) | XP_011542078.1:n.161-2823T>C | |
| XM_011543777.1:c.161-2832T>C (VCAN-AS1) | XP_011542079.1:n.161-2832T>C | |
| XM_011543778.1:c.161-2823T>C (VCAN-AS1) | XP_011542080.1:n.161-2823T>C | |
| XM_011543779.1:c.161-2823T>C (VCAN-AS1) | XP_011542081.1:n.161-2823T>C | |
| XM_011543780.1:c.13-2832T>C (VCAN-AS1) | XP_011542082.1:n.13-2832T>C | |
| XM_011543781.1:c.161-2823T>C (VCAN-AS1) | XP_011542083.1:n.161-2823T>C | |
| XM_011543782.1:c.161-2823T>C (VCAN-AS1) | XP_011542084.1:n.161-2823T>C | |
| XR_948512.1:n.471-2823T>C (VCAN-AS1) | ||
| XR_948513.1:n.471-2832T>C (VCAN-AS1) | ||
| XR_948514.1:n.471-2823T>C (VCAN-AS1) | ||
| XR_948515.1:n.471-2832T>C (VCAN-AS1) | ||
| XR_948516.1:n.471-2832T>C (VCAN-AS1) | ||
| NR_136215.1:n.285-2832T>C (VCAN-AS1) | ||
| NM_004385.5:c.4004-2A>G (VCAN) MANE Select | NP_004376.2:n.4004-2A>G | |
| NM_001126336.3:c.1043-8532A>G (VCAN) | NP_001119808.1:n.1043-8532A>G | |
| NM_001164097.2:c.1043-2A>G (VCAN) | NP_001157569.1:n.1043-2A>G | |
| NM_001164098.2:c.4004-8532A>G (VCAN) | NP_001157570.1:n.4004-8532A>G |