Canonical Allele Identifier: CA393727020

Gene: ACAN

Linked Data

• MyVariant Identifiers: chr15:g.89402142C>A (hg19) ; chr15:g.88858911C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88858911C>A , CM000677.2:g.88858911C>A	GRCh38
NC_000015.9:g.89402142C>A , CM000677.1:g.89402142C>A	GRCh37
NC_000015.8:g.87203146C>A	NCBI36
NG_012794.1:g.60469C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000439576.7:c.6326C>A	ENSP00000387356.2:p.Ala2109Asp
ENST00000560601.4:c.6326C>A MANE Select	ENSP00000453581.2:p.Ala2109Asp
ENST00000561243.7:c.6326C>A	ENSP00000453342.3:p.Ala2109Asp
ENST00000352105.11:c.6326C>A	ENSP00000341615.7:p.Ala2109Asp
ENST00000439576.6:c.6326C>A	ENSP00000387356.2:p.Ala2109Asp
ENST00000559004.5:c.6326C>A	ENSP00000453499.1:p.Ala2109Asp
ENST00000561243.5:c.6326C>A	ENSP00000453342.1:p.Ala2109Asp
ENST00000617301.4:c.6269C>A	ENSP00000484456.1:p.Ala2090Asp
NM_001135.3:c.6326C>A	NP_001126.3:p.Ala2109Asp
NM_013227.3:c.6326C>A	NP_037359.3:p.Ala2109Asp
XM_006720419.1:c.6326C>A	XP_006720482.1:p.Ala2109Asp
XM_011521313.1:c.6326C>A	XP_011519615.1:p.Ala2109Asp
XM_011521314.1:c.6326C>A	XP_011519616.1:p.Ala2109Asp
NM_001369268.1:c.6326C>A MANE Select	NP_001356197.1:p.Ala2109Asp
NM_001135.4:c.6326C>A	NP_001126.3:p.Ala2109Asp
NM_013227.4:c.6326C>A	NP_037359.3:p.Ala2109Asp