Canonical Allele Identifier: CA360293196

Gene: VCAN

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83483564A>G , CM000667.2:g.83483564A>G	GRCh38
NC_000005.9:g.82779383A>G , CM000667.1:g.82779383A>G	GRCh37
NC_000005.8:g.82815139A>G	NCBI36
NG_012682.1:g.16854A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004385.5:c.46A>G MANE Select	NP_004376.2:p.Ile16Val
ENST00000265077.8:c.46A>G MANE Select	ENSP00000265077.3:p.Ile16Val
NM_001126336.2:c.46A>G	NP_001119808.1:p.Ile16Val
NM_001126336.3:c.46A>G	NP_001119808.1:p.Ile16Val
NM_001164097.1:c.46A>G	NP_001157569.1:p.Ile16Val
NM_001164097.2:c.46A>G	NP_001157569.1:p.Ile16Val
NM_001164098.1:c.46A>G	NP_001157570.1:p.Ile16Val
NM_001164098.2:c.46A>G	NP_001157570.1:p.Ile16Val
NM_004385.4:c.46A>G	NP_004376.2:p.Ile16Val
ENST00000265077.7:c.46A>G	ENSP00000265077.3:p.Ile16Val
ENST00000342785.8:c.46A>G	ENSP00000342768.4:p.Ile16Val
ENST00000343200.9:c.46A>G	ENSP00000340062.5:p.Ile16Val
ENST00000502527.2:c.46A>G	ENSP00000421362.2:p.Ile16Val
ENST00000503923.1:n.458A>G
ENST00000512590.6:c.-99A>G	ENSP00000425959.2:n.-99A>G
ENST00000513960.5:c.46A>G	ENSP00000426251.1:p.Ile16Val
ENST00000513984.5:c.46A>G	ENSP00000426715.1:p.Ile16Val