Canonical Allele Identifier: CA3332442

Gene: VCAN

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83490420C>T , CM000667.2:g.83490420C>T	GRCh38
NC_000005.9:g.82786239C>T , CM000667.1:g.82786239C>T	GRCh37
NC_000005.8:g.82821995C>T	NCBI36
NG_012682.1:g.23710C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004385.5:c.393C>T MANE Select	NP_004376.2:p.Asp131=
ENST00000265077.8:c.393C>T MANE Select	ENSP00000265077.3:p.Asp131=
NM_001126336.2:c.393C>T	NP_001119808.1:p.Asp131=
NM_001126336.3:c.393C>T	NP_001119808.1:p.Asp131=
NM_001164097.1:c.393C>T	NP_001157569.1:p.Asp131=
NM_001164097.2:c.393C>T	NP_001157569.1:p.Asp131=
NM_001164098.1:c.393C>T	NP_001157570.1:p.Asp131=
NM_001164098.2:c.393C>T	NP_001157570.1:p.Asp131=
NM_004385.4:c.393C>T	NP_004376.2:p.Asp131=
ENST00000265077.7:c.393C>T	ENSP00000265077.3:p.Asp131=
ENST00000342785.8:c.393C>T	ENSP00000342768.4:p.Asp131=
ENST00000343200.9:c.393C>T	ENSP00000340062.5:p.Asp131=
ENST00000502527.2:c.393C>T	ENSP00000421362.2:p.Asp131=
ENST00000512590.6:c.249C>T	ENSP00000425959.2:p.Asp83=
ENST00000513960.5:c.393C>T	ENSP00000426251.1:p.Asp131=
ENST00000513984.5:c.393C>T	ENSP00000426715.1:p.Asp131=