Canonical Allele Identifier: CA1078170918
Gene: VCAN HGNC NCBI

Linked Data

dbSNP Id: rs1490731059
gnomAD v3: 5-83498146-G-A
gnomAD v4: 5-83498146-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.83498146G>A , CM000667.2:g.83498146G>A GRCh38
NC_000005.9:g.82793965G>A , CM000667.1:g.82793965G>A GRCh37
NC_000005.8:g.82829721G>A NCBI36
NG_012682.1:g.31436G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265077.8:c.748+4215G>A MANE Select ENSP00000265077.3:n.748+4215G>A
ENST00000265077.7:c.748+4215G>A ENSP00000265077.3:n.748+4215G>A
ENST00000342785.8:c.748+4215G>A ENSP00000342768.4:n.748+4215G>A
ENST00000343200.9:c.748+4215G>A ENSP00000340062.5:n.748+4215G>A
ENST00000502527.2:c.748+4215G>A ENSP00000421362.2:n.748+4215G>A
ENST00000512590.6:c.604+4215G>A ENSP00000425959.2:n.604+4215G>A
ENST00000513960.5:c.748+4215G>A ENSP00000426251.1:n.748+4215G>A
ENST00000513984.5:c.748+4215G>A ENSP00000426715.1:n.748+4215G>A
NM_001126336.2:c.748+4215G>A NP_001119808.1:n.748+4215G>A
NM_001164097.1:c.748+4215G>A NP_001157569.1:n.748+4215G>A
NM_001164098.1:c.748+4215G>A NP_001157570.1:n.748+4215G>A
NM_004385.4:c.748+4215G>A NP_004376.2:n.748+4215G>A
NM_004385.5:c.748+4215G>A MANE Select NP_004376.2:n.748+4215G>A
NM_001126336.3:c.748+4215G>A NP_001119808.1:n.748+4215G>A
NM_001164097.2:c.748+4215G>A NP_001157569.1:n.748+4215G>A
NM_001164098.2:c.748+4215G>A NP_001157570.1:n.748+4215G>A