Canonical Allele Identifier: CA3333665
Gene: VCAN HGNC NCBI
VCAN-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.83540584C>T , CM000667.2:g.83540584C>T GRCh38
NC_000005.9:g.82836403C>T , CM000667.1:g.82836403C>T GRCh37
NC_000005.8:g.82872159C>T NCBI36
NG_012682.1:g.73874C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265077.8:c.7581C>T (VCAN) MANE Select ENSP00000265077.3:p.Phe2527=
ENST00000265077.7:c.7581C>T (VCAN) ENSP00000265077.3:p.Phe2527=
ENST00000342785.8:c.4004-4953C>T (VCAN) ENSP00000342768.4:n.4004-4953C>T
ENST00000343200.9:c.4620C>T (VCAN) ENSP00000340062.5:p.Phe1540=
ENST00000502527.2:c.1043-4953C>T (VCAN) ENSP00000421362.2:n.1043-4953C>T
ENST00000512590.6:c.3860-4953C>T (VCAN) ENSP00000425959.2:n.3860-4953C>T
ENST00000513016.5:n.4971C>T (VCAN)
NM_001126336.2:c.1043-4953C>T (VCAN) NP_001119808.1:n.1043-4953C>T
NM_001164097.1:c.4620C>T (VCAN) NP_001157569.1:p.Phe1540=
NM_001164098.1:c.4004-4953C>T (VCAN) NP_001157570.1:n.4004-4953C>T
NM_004385.4:c.7581C>T (VCAN) NP_004376.2:p.Phe2527=
XM_011543776.1:c.161-6402G>A (VCAN-AS1) XP_011542078.1:n.161-6402G>A
XM_011543777.1:c.161-6411G>A (VCAN-AS1) XP_011542079.1:n.161-6411G>A
XM_011543778.1:c.161-6402G>A (VCAN-AS1) XP_011542080.1:n.161-6402G>A
XM_011543779.1:c.161-6402G>A (VCAN-AS1) XP_011542081.1:n.161-6402G>A
XM_011543780.1:c.13-6411G>A (VCAN-AS1) XP_011542082.1:n.13-6411G>A
XM_011543781.1:c.161-6402G>A (VCAN-AS1) XP_011542083.1:n.161-6402G>A
XM_011543782.1:c.161-6402G>A (VCAN-AS1) XP_011542084.1:n.161-6402G>A
XR_948512.1:n.471-6402G>A (VCAN-AS1)
XR_948513.1:n.471-6411G>A (VCAN-AS1)
XR_948514.1:n.471-6402G>A (VCAN-AS1)
XR_948515.1:n.471-6411G>A (VCAN-AS1)
XR_948516.1:n.471-6411G>A (VCAN-AS1)
NR_136215.1:n.285-6411G>A (VCAN-AS1)
NM_004385.5:c.7581C>T (VCAN) MANE Select NP_004376.2:p.Phe2527=
NM_001126336.3:c.1043-4953C>T (VCAN) NP_001119808.1:n.1043-4953C>T
NM_001164097.2:c.4620C>T (VCAN) NP_001157569.1:p.Phe1540=
NM_001164098.2:c.4004-4953C>T (VCAN) NP_001157570.1:n.4004-4953C>T