Canonical Allele Identifier: CA3333749
Gene: VCAN HGNC NCBI
VCAN-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.83541093G>A , CM000667.2:g.83541093G>A GRCh38
NC_000005.9:g.82836912G>A , CM000667.1:g.82836912G>A GRCh37
NC_000005.8:g.82872668G>A NCBI36
NG_012682.1:g.74383G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004385.5:c.8090G>A (VCAN) MANE Select NP_004376.2:p.Arg2697His
ENST00000265077.8:c.8090G>A (VCAN) MANE Select ENSP00000265077.3:p.Arg2697His
NM_001126336.2:c.1043-4444G>A (VCAN) NP_001119808.1:n.1043-4444G>A
NM_001126336.3:c.1043-4444G>A (VCAN) NP_001119808.1:n.1043-4444G>A
NM_001164097.1:c.5129G>A (VCAN) NP_001157569.1:p.Arg1710His
NM_001164097.2:c.5129G>A (VCAN) NP_001157569.1:p.Arg1710His
NM_001164098.1:c.4004-4444G>A (VCAN) NP_001157570.1:n.4004-4444G>A
NM_001164098.2:c.4004-4444G>A (VCAN) NP_001157570.1:n.4004-4444G>A
NM_004385.4:c.8090G>A (VCAN) NP_004376.2:p.Arg2697His
NR_136215.1:n.285-6920C>T (VCAN-AS1)
ENST00000265077.7:c.8090G>A (VCAN) ENSP00000265077.3:p.Arg2697His
ENST00000342785.8:c.4004-4444G>A (VCAN) ENSP00000342768.4:n.4004-4444G>A
ENST00000343200.9:c.5129G>A (VCAN) ENSP00000340062.5:p.Arg1710His
ENST00000502527.2:c.1043-4444G>A (VCAN) ENSP00000421362.2:n.1043-4444G>A
ENST00000512590.6:c.3860-4444G>A (VCAN) ENSP00000425959.2:n.3860-4444G>A
ENST00000513016.5:n.5480G>A (VCAN)
XM_011543776.1:c.161-6911C>T (VCAN-AS1) XP_011542078.1:n.161-6911C>T
XM_011543777.1:c.161-6920C>T (VCAN-AS1) XP_011542079.1:n.161-6920C>T
XM_011543778.1:c.161-6911C>T (VCAN-AS1) XP_011542080.1:n.161-6911C>T
XM_011543779.1:c.161-6911C>T (VCAN-AS1) XP_011542081.1:n.161-6911C>T
XM_011543780.1:c.13-6920C>T (VCAN-AS1) XP_011542082.1:n.13-6920C>T
XM_011543781.1:c.161-6911C>T (VCAN-AS1) XP_011542083.1:n.161-6911C>T
XM_011543782.1:c.161-6911C>T (VCAN-AS1) XP_011542084.1:n.161-6911C>T
XR_948512.1:n.471-6911C>T (VCAN-AS1)
XR_948513.1:n.471-6920C>T (VCAN-AS1)
XR_948514.1:n.471-6911C>T (VCAN-AS1)
XR_948515.1:n.471-6920C>T (VCAN-AS1)
XR_948516.1:n.471-6920C>T (VCAN-AS1)