Canonical Allele Identifier: CA1559748743

Gene: VCAN

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83498270C= , CM000667.2:g.83498270C=	GRCh38
NC_000005.9:g.82794089C= , CM000667.1:g.82794089C=	GRCh37
NC_000005.8:g.82829845C=	NCBI36
NG_012682.1:g.31560C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265077.8:c.748+4339C= MANE Select	ENSP00000265077.3:n.748+4339C=
ENST00000265077.7:c.748+4339C=	ENSP00000265077.3:n.748+4339C=
ENST00000342785.8:c.748+4339C=	ENSP00000342768.4:n.748+4339C=
ENST00000343200.9:c.748+4339C=	ENSP00000340062.5:n.748+4339C=
ENST00000502527.2:c.748+4339C=	ENSP00000421362.2:n.748+4339C=
ENST00000512590.6:c.604+4339C=	ENSP00000425959.2:n.604+4339C=
ENST00000513960.5:c.748+4339C=	ENSP00000426251.1:n.748+4339C=
ENST00000513984.5:c.748+4339C=	ENSP00000426715.1:n.748+4339C=
NM_001126336.2:c.748+4339C=	NP_001119808.1:n.748+4339C=
NM_001164097.1:c.748+4339C=	NP_001157569.1:n.748+4339C=
NM_001164098.1:c.748+4339C=	NP_001157570.1:n.748+4339C=
NM_004385.4:c.748+4339C=	NP_004376.2:n.748+4339C=
NM_004385.5:c.748+4339C= MANE Select	NP_004376.2:n.748+4339C=
NM_001126336.3:c.748+4339C=	NP_001119808.1:n.748+4339C=
NM_001164097.2:c.748+4339C=	NP_001157569.1:n.748+4339C=
NM_001164098.2:c.748+4339C=	NP_001157570.1:n.748+4339C=