Canonical Allele Identifier: CA3333687

Gene: VCAN VCAN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83540746T>C , CM000667.2:g.83540746T>C	GRCh38
NC_000005.9:g.82836565T>C , CM000667.1:g.82836565T>C	GRCh37
NC_000005.8:g.82872321T>C	NCBI36
NG_012682.1:g.74036T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265077.8:c.7743T>C (VCAN) MANE Select	ENSP00000265077.3:p.Asp2581=
ENST00000265077.7:c.7743T>C (VCAN)	ENSP00000265077.3:p.Asp2581=
ENST00000342785.8:c.4004-4791T>C (VCAN)	ENSP00000342768.4:n.4004-4791T>C
ENST00000343200.9:c.4782T>C (VCAN)	ENSP00000340062.5:p.Asp1594=
ENST00000502527.2:c.1043-4791T>C (VCAN)	ENSP00000421362.2:n.1043-4791T>C
ENST00000512590.6:c.3860-4791T>C (VCAN)	ENSP00000425959.2:n.3860-4791T>C
ENST00000513016.5:n.5133T>C (VCAN)
NM_001126336.2:c.1043-4791T>C (VCAN)	NP_001119808.1:n.1043-4791T>C
NM_001164097.1:c.4782T>C (VCAN)	NP_001157569.1:p.Asp1594=
NM_001164098.1:c.4004-4791T>C (VCAN)	NP_001157570.1:n.4004-4791T>C
NM_004385.4:c.7743T>C (VCAN)	NP_004376.2:p.Asp2581=
XM_011543776.1:c.161-6564A>G (VCAN-AS1)	XP_011542078.1:n.161-6564A>G
XM_011543777.1:c.161-6573A>G (VCAN-AS1)	XP_011542079.1:n.161-6573A>G
XM_011543778.1:c.161-6564A>G (VCAN-AS1)	XP_011542080.1:n.161-6564A>G
XM_011543779.1:c.161-6564A>G (VCAN-AS1)	XP_011542081.1:n.161-6564A>G
XM_011543780.1:c.13-6573A>G (VCAN-AS1)	XP_011542082.1:n.13-6573A>G
XM_011543781.1:c.161-6564A>G (VCAN-AS1)	XP_011542083.1:n.161-6564A>G
XM_011543782.1:c.161-6564A>G (VCAN-AS1)	XP_011542084.1:n.161-6564A>G
XR_948512.1:n.471-6564A>G (VCAN-AS1)
XR_948513.1:n.471-6573A>G (VCAN-AS1)
XR_948514.1:n.471-6564A>G (VCAN-AS1)
XR_948515.1:n.471-6573A>G (VCAN-AS1)
XR_948516.1:n.471-6573A>G (VCAN-AS1)
NR_136215.1:n.285-6573A>G (VCAN-AS1)
NM_004385.5:c.7743T>C (VCAN) MANE Select	NP_004376.2:p.Asp2581=
NM_001126336.3:c.1043-4791T>C (VCAN)	NP_001119808.1:n.1043-4791T>C
NM_001164097.2:c.4782T>C (VCAN)	NP_001157569.1:p.Asp1594=
NM_001164098.2:c.4004-4791T>C (VCAN)	NP_001157570.1:n.4004-4791T>C