Canonical Allele Identifier: CA2194343536
Gene: ACAN HGNC NCBI

Linked Data

dbSNP Id: rs1897126634

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.88858807dup , CM000677.2:g.88858807dup GRCh38
NC_000015.9:g.89402038dup , CM000677.1:g.89402038dup GRCh37
NC_000015.8:g.87203042dup NCBI36
NG_012794.1:g.60365dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000439576.7:c.6222dup ENSP00000387356.2:p.Thr2075HisfsTer6
ENST00000560601.4:c.6222dup MANE Select ENSP00000453581.2:p.Thr2075HisfsTer6
ENST00000561243.7:c.6222dup ENSP00000453342.3:p.Thr2075HisfsTer6
ENST00000352105.11:c.6222dup ENSP00000341615.7:p.Thr2075HisfsTer6
ENST00000439576.6:c.6222dup ENSP00000387356.2:p.Thr2075HisfsTer6
ENST00000559004.5:c.6222dup ENSP00000453499.1:p.Thr2075HisfsTer6
ENST00000561243.5:c.6222dup ENSP00000453342.1:p.Thr2075HisfsTer6
ENST00000617301.4:c.6165dup ENSP00000484456.1:p.Thr2056HisfsTer6
NM_001135.3:c.6222dup NP_001126.3:p.Thr2075HisfsTer6
NM_013227.3:c.6222dup NP_037359.3:p.Thr2075HisfsTer6
XM_006720419.1:c.6222dup XP_006720482.1:p.Thr2075HisfsTer6
XM_011521313.1:c.6222dup XP_011519615.1:p.Thr2075HisfsTer6
XM_011521314.1:c.6222dup XP_011519616.1:p.Thr2075HisfsTer6
NM_001369268.1:c.6222dup MANE Select NP_001356197.1:p.Thr2075HisfsTer6
NM_001135.4:c.6222dup NP_001126.3:p.Thr2075HisfsTer6
NM_013227.4:c.6222dup NP_037359.3:p.Thr2075HisfsTer6