Canonical Allele Identifier: CA274470646
Gene: ACAN HGNC NCBI

Linked Data

dbSNP Id: rs1054868950

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.88845677C>A , CM000677.2:g.88845677C>A GRCh38
NC_000015.9:g.89388908C>A , CM000677.1:g.89388908C>A GRCh37
NC_000015.8:g.87189912C>A NCBI36
NG_012794.1:g.47235C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000439576.7:c.1224C>A ENSP00000387356.2:p.Ser408=
ENST00000560601.4:c.1224C>A MANE Select ENSP00000453581.2:p.Ser408=
ENST00000561243.7:c.1224C>A ENSP00000453342.3:p.Ser408=
ENST00000352105.11:c.1224C>A ENSP00000341615.7:p.Ser408=
ENST00000439576.6:c.1224C>A ENSP00000387356.2:p.Ser408=
ENST00000558207.5:c.1224C>A ENSP00000453003.1:p.Ser408=
ENST00000559004.5:c.1224C>A ENSP00000453499.1:p.Ser408=
ENST00000561243.5:c.1224C>A ENSP00000453342.1:p.Ser408=
ENST00000617301.4:c.1224C>A ENSP00000484456.1:p.Ser408=
NM_001135.3:c.1224C>A NP_001126.3:p.Ser408=
NM_013227.3:c.1224C>A NP_037359.3:p.Ser408=
XM_006720419.1:c.1224C>A XP_006720482.1:p.Ser408=
XM_011521313.1:c.1224C>A XP_011519615.1:p.Ser408=
XM_011521314.1:c.1224C>A XP_011519616.1:p.Ser408=
NM_001369268.1:c.1224C>A MANE Select NP_001356197.1:p.Ser408=
NM_001135.4:c.1224C>A NP_001126.3:p.Ser408=
NM_013227.4:c.1224C>A NP_037359.3:p.Ser408=