Canonical Allele Identifier: CA393726657

Gene: ACAN

Linked Data

• dbSNP Id: rs1247259711
• MyVariant Identifiers: chr15:g.89401967T>A (hg19) ; chr15:g.88858736T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88858736T>A , CM000677.2:g.88858736T>A	GRCh38
NC_000015.9:g.89401967T>A , CM000677.1:g.89401967T>A	GRCh37
NC_000015.8:g.87202971T>A	NCBI36
NG_012794.1:g.60294T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439576.7:c.6151T>A	ENSP00000387356.2:p.Ser2051Thr
ENST00000560601.4:c.6151T>A MANE Select	ENSP00000453581.2:p.Ser2051Thr
ENST00000561243.7:c.6151T>A	ENSP00000453342.3:p.Ser2051Thr
ENST00000352105.11:c.6151T>A	ENSP00000341615.7:p.Ser2051Thr
ENST00000439576.6:c.6151T>A	ENSP00000387356.2:p.Ser2051Thr
ENST00000559004.5:c.6151T>A	ENSP00000453499.1:p.Ser2051Thr
ENST00000561243.5:c.6151T>A	ENSP00000453342.1:p.Ser2051Thr
ENST00000617301.4:c.6094T>A	ENSP00000484456.1:p.Ser2032Thr
NM_001135.3:c.6151T>A	NP_001126.3:p.Ser2051Thr
NM_013227.3:c.6151T>A	NP_037359.3:p.Ser2051Thr
XM_006720419.1:c.6151T>A	XP_006720482.1:p.Ser2051Thr
XM_011521313.1:c.6151T>A	XP_011519615.1:p.Ser2051Thr
XM_011521314.1:c.6151T>A	XP_011519616.1:p.Ser2051Thr
NM_001369268.1:c.6151T>A MANE Select	NP_001356197.1:p.Ser2051Thr
NM_001135.4:c.6151T>A	NP_001126.3:p.Ser2051Thr
NM_013227.4:c.6151T>A	NP_037359.3:p.Ser2051Thr