Canonical Allele Identifier: CA7719497
Gene: ACAN HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs16942341

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.88845674C>T , CM000677.2:g.88845674C>T GRCh38
NC_000015.9:g.89388905C>T , CM000677.1:g.89388905C>T GRCh37
NC_000015.8:g.87189909C>T NCBI36
NG_012794.1:g.47232C>T

Transcript Alleles

HGVS Amino-acid change
NM_001135.3:c.1221C>T VV NP_001126.3:p.Val407=
NM_013227.3:c.1221C>T VV NP_037359.3:p.Val407=
XM_006720419.1:c.1221C>T XP_006720482.1:p.Val407=
XM_011521313.1:c.1221C>T XP_011519615.1:p.Val407=
XM_011521314.1:c.1221C>T XP_011519616.1:p.Val407=
ENST00000352105.11:c.1221C>T ENSP00000341615.7:p.Val407=
ENST00000439576.6:c.1221C>T ENSP00000387356.2:p.Val407=
ENST00000558207.5:c.1221C>T ENSP00000453003.1:p.Val407=
ENST00000559004.5:c.1221C>T ENSP00000453499.1:p.Val407=
ENST00000561243.5:n.1221C>T ENSP00000453342.1:p.Val407=
ENST00000617301.4:c.1221C>T ENSP00000484456.1:p.Val407=