Canonical Allele Identifier: CA1559738572

Gene: VCAN VCAN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83515566A= , CM000667.2:g.83515566A=	GRCh38
NC_000005.9:g.82811385A= , CM000667.1:g.82811385A=	GRCh37
NC_000005.8:g.82847141A=	NCBI36
NG_012682.1:g.48856A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265077.8:c.1042+3170A= (VCAN) MANE Select	ENSP00000265077.3:n.1042+3170A=
ENST00000265077.7:c.1042+3170A= (VCAN)	ENSP00000265077.3:n.1042+3170A=
ENST00000342785.8:c.1042+3170A= (VCAN)	ENSP00000342768.4:n.1042+3170A=
ENST00000343200.9:c.1042+3170A= (VCAN)	ENSP00000340062.5:n.1042+3170A=
ENST00000502527.2:c.1042+3170A= (VCAN)	ENSP00000421362.2:n.1042+3170A=
ENST00000512590.6:c.898+3170A= (VCAN)	ENSP00000425959.2:n.898+3170A=
ENST00000513960.5:c.1042+3170A= (VCAN)	ENSP00000426251.1:n.1042+3170A=
ENST00000515397.1:n.295+3170A= (VCAN)
NM_001126336.2:c.1042+3170A= (VCAN)	NP_001119808.1:n.1042+3170A=
NM_001164097.1:c.1042+3170A= (VCAN)	NP_001157569.1:n.1042+3170A=
NM_001164098.1:c.1042+3170A= (VCAN)	NP_001157570.1:n.1042+3170A=
NM_004385.4:c.1042+3170A= (VCAN)	NP_004376.2:n.1042+3170A=
XM_011543776.1:c.454-1910T= (VCAN-AS1)	XP_011542078.1:n.454-1910T=
XM_011543777.1:c.445-1910T= (VCAN-AS1)	XP_011542079.1:n.445-1910T=
XM_011543778.1:c.454-1910T= (VCAN-AS1)	XP_011542080.1:n.454-1910T=
XM_011543779.1:c.482-1910T= (VCAN-AS1)	XP_011542081.1:n.482-1910T=
XM_011543780.1:c.250-1910T= (VCAN-AS1)	XP_011542082.1:n.250-1910T=
XM_011543781.1:c.454-5646T= (VCAN-AS1)	XP_011542083.1:n.454-5646T=
XM_011543782.1:c.320-1910T= (VCAN-AS1)	XP_011542084.1:n.320-1910T=
XR_948512.1:n.839-1910T= (VCAN-AS1)
XR_948517.1:n.181-1910T= (VCAN-AS1)
NM_004385.5:c.1042+3170A= (VCAN) MANE Select	NP_004376.2:n.1042+3170A=
NM_001126336.3:c.1042+3170A= (VCAN)	NP_001119808.1:n.1042+3170A=
NM_001164097.2:c.1042+3170A= (VCAN)	NP_001157569.1:n.1042+3170A=
NM_001164098.2:c.1042+3170A= (VCAN)	NP_001157570.1:n.1042+3170A=