Canonical Allele Identifier: CA121810469

Gene: VCAN VCAN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83539730A>G , CM000667.2:g.83539730A>G	GRCh38
NC_000005.9:g.82835549A>G , CM000667.1:g.82835549A>G	GRCh37
NC_000005.8:g.82871305A>G	NCBI36
NG_012682.1:g.73020A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265077.8:c.6727A>G (VCAN) MANE Select	ENSP00000265077.3:p.Thr2243Ala
ENST00000265077.7:c.6727A>G (VCAN)	ENSP00000265077.3:p.Thr2243Ala
ENST00000342785.8:c.4004-5807A>G (VCAN)	ENSP00000342768.4:n.4004-5807A>G
ENST00000343200.9:c.3766A>G (VCAN)	ENSP00000340062.5:p.Thr1256Ala
ENST00000502527.2:c.1043-5807A>G (VCAN)	ENSP00000421362.2:n.1043-5807A>G
ENST00000512590.6:c.3860-5807A>G (VCAN)	ENSP00000425959.2:n.3860-5807A>G
ENST00000513016.5:n.4117A>G (VCAN)
NM_001126336.2:c.1043-5807A>G (VCAN)	NP_001119808.1:n.1043-5807A>G
NM_001164097.1:c.3766A>G (VCAN)	NP_001157569.1:p.Thr1256Ala
NM_001164098.1:c.4004-5807A>G (VCAN)	NP_001157570.1:n.4004-5807A>G
NM_004385.4:c.6727A>G (VCAN)	NP_004376.2:p.Thr2243Ala
XM_011543776.1:c.161-5548T>C (VCAN-AS1)	XP_011542078.1:n.161-5548T>C
XM_011543777.1:c.161-5557T>C (VCAN-AS1)	XP_011542079.1:n.161-5557T>C
XM_011543778.1:c.161-5548T>C (VCAN-AS1)	XP_011542080.1:n.161-5548T>C
XM_011543779.1:c.161-5548T>C (VCAN-AS1)	XP_011542081.1:n.161-5548T>C
XM_011543780.1:c.13-5557T>C (VCAN-AS1)	XP_011542082.1:n.13-5557T>C
XM_011543781.1:c.161-5548T>C (VCAN-AS1)	XP_011542083.1:n.161-5548T>C
XM_011543782.1:c.161-5548T>C (VCAN-AS1)	XP_011542084.1:n.161-5548T>C
XR_948512.1:n.471-5548T>C (VCAN-AS1)
XR_948513.1:n.471-5557T>C (VCAN-AS1)
XR_948514.1:n.471-5548T>C (VCAN-AS1)
XR_948515.1:n.471-5557T>C (VCAN-AS1)
XR_948516.1:n.471-5557T>C (VCAN-AS1)
NR_136215.1:n.285-5557T>C (VCAN-AS1)
NM_004385.5:c.6727A>G (VCAN) MANE Select	NP_004376.2:p.Thr2243Ala
NM_001126336.3:c.1043-5807A>G (VCAN)	NP_001119808.1:n.1043-5807A>G
NM_001164097.2:c.3766A>G (VCAN)	NP_001157569.1:p.Thr1256Ala
NM_001164098.2:c.4004-5807A>G (VCAN)	NP_001157570.1:n.4004-5807A>G