Canonical Allele Identifier: CA3334068

Gene: VCAN VCAN-AS1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83554989A>G , CM000667.2:g.83554989A>G	GRCh38
NC_000005.9:g.82850808A>G , CM000667.1:g.82850808A>G	GRCh37
NC_000005.8:g.82886564A>G	NCBI36
NG_012682.1:g.88279A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265077.8:c.9686A>G (VCAN) MANE Select	ENSP00000265077.3:p.Asn3229Ser
ENST00000265077.7:c.9686A>G (VCAN)	ENSP00000265077.3:p.Asn3229Ser
ENST00000342785.8:c.4424A>G (VCAN)	ENSP00000342768.4:p.Asn1475Ser
ENST00000343200.9:c.6725A>G (VCAN)	ENSP00000340062.5:p.Asn2242Ser
ENST00000502527.2:c.1463A>G (VCAN)	ENSP00000421362.2:p.Asn488Ser
ENST00000505615.1:n.195A>G (VCAN)
ENST00000512590.6:c.4280A>G (VCAN)	ENSP00000425959.2:p.Asn1427Ser
ENST00000513016.5:n.7076A>G (VCAN)
NM_001126336.2:c.1463A>G (VCAN)	NP_001119808.1:p.Asn488Ser
NM_001164097.1:c.6725A>G (VCAN)	NP_001157569.1:p.Asn2242Ser
NM_001164098.1:c.4424A>G (VCAN)	NP_001157570.1:p.Asn1475Ser
NM_004385.4:c.9686A>G (VCAN)	NP_004376.2:p.Asn3229Ser
XM_011543776.1:c.160+6542T>C (VCAN-AS1)	XP_011542078.1:n.160+6542T>C
XM_011543777.1:c.160+6542T>C (VCAN-AS1)	XP_011542079.1:n.160+6542T>C
XM_011543778.1:c.160+6542T>C (VCAN-AS1)	XP_011542080.1:n.160+6542T>C
XM_011543779.1:c.160+6542T>C (VCAN-AS1)	XP_011542081.1:n.160+6542T>C
XM_011543780.1:c.12+211T>C (VCAN-AS1)	XP_011542082.1:n.12+211T>C
XM_011543781.1:c.160+6542T>C (VCAN-AS1)	XP_011542083.1:n.160+6542T>C
XM_011543782.1:c.160+6542T>C (VCAN-AS1)	XP_011542084.1:n.160+6542T>C
XR_948512.1:n.470+6542T>C (VCAN-AS1)
XR_948513.1:n.470+6542T>C (VCAN-AS1)
XR_948514.1:n.470+6542T>C (VCAN-AS1)
XR_948515.1:n.470+6542T>C (VCAN-AS1)
XR_948516.1:n.470+6542T>C (VCAN-AS1)
NR_136215.1:n.284+7042T>C (VCAN-AS1)
NM_004385.5:c.9686A>G (VCAN) MANE Select	NP_004376.2:p.Asn3229Ser
NM_001126336.3:c.1463A>G (VCAN)	NP_001119808.1:p.Asn488Ser
NM_001164097.2:c.6725A>G (VCAN)	NP_001157569.1:p.Asn2242Ser
NM_001164098.2:c.4424A>G (VCAN)	NP_001157570.1:p.Asn1475Ser