Canonical Allele Identifier: CA2630217247

Gene: ACAN

Linked Data

• gnomAD v4: 15-88845493-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88845493C>A , CM000677.2:g.88845493C>A	GRCh38
NC_000015.9:g.89388724C>A , CM000677.1:g.89388724C>A	GRCh37
NC_000015.8:g.87189728C>A	NCBI36
NG_012794.1:g.47051C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000439576.7:c.1052-12C>A	ENSP00000387356.2:n.1052-12C>A
ENST00000560601.4:c.1052-12C>A MANE Select	ENSP00000453581.2:n.1052-12C>A
ENST00000561243.7:c.1052-12C>A	ENSP00000453342.3:n.1052-12C>A
ENST00000352105.11:c.1052-12C>A	ENSP00000341615.7:n.1052-12C>A
ENST00000439576.6:c.1052-12C>A	ENSP00000387356.2:n.1052-12C>A
ENST00000558207.5:c.1052-12C>A	ENSP00000453003.1:n.1052-12C>A
ENST00000559004.5:c.1052-12C>A	ENSP00000453499.1:n.1052-12C>A
ENST00000561243.5:c.1052-12C>A	ENSP00000453342.1:n.1052-12C>A
ENST00000617301.4:c.1052-12C>A	ENSP00000484456.1:n.1052-12C>A
NM_001135.3:c.1052-12C>A	NP_001126.3:n.1052-12C>A
NM_013227.3:c.1052-12C>A	NP_037359.3:n.1052-12C>A
XM_006720419.1:c.1052-12C>A	XP_006720482.1:n.1052-12C>A
XM_011521313.1:c.1052-12C>A	XP_011519615.1:n.1052-12C>A
XM_011521314.1:c.1052-12C>A	XP_011519616.1:n.1052-12C>A
NM_001369268.1:c.1052-12C>A MANE Select	NP_001356197.1:n.1052-12C>A
NM_001135.4:c.1052-12C>A	NP_001126.3:n.1052-12C>A
NM_013227.4:c.1052-12C>A	NP_037359.3:n.1052-12C>A