Canonical Allele Identifier: CA716875621

Gene: ACAN

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88816458T>G , CM000677.2:g.88816458T>G	GRCh38
NC_000015.9:g.89359689T>G , CM000677.1:g.89359689T>G	GRCh37
NC_000015.8:g.87160693T>G	NCBI36
NG_012794.1:g.18016T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439576.7:c.-8+12649T>G	ENSP00000387356.2:n.-8+12649T>G
ENST00000560601.4:c.-8+12649T>G MANE Select	ENSP00000453581.2:n.-8+12649T>G
ENST00000561243.7:c.-8+12649T>G	ENSP00000453342.3:n.-8+12649T>G
ENST00000352105.11:c.-8+12649T>G	ENSP00000341615.7:n.-8+12649T>G
ENST00000439576.6:c.-8+12649T>G	ENSP00000387356.2:n.-8+12649T>G
ENST00000558207.5:c.-8+12649T>G	ENSP00000453003.1:n.-8+12649T>G
ENST00000559004.5:c.-8+12649T>G	ENSP00000453499.1:n.-8+12649T>G
ENST00000617301.4:c.-8+12649T>G	ENSP00000484456.1:n.-8+12649T>G
NM_001135.3:c.-8+12649T>G	NP_001126.3:n.-8+12649T>G
NM_013227.3:c.-8+12649T>G	NP_037359.3:n.-8+12649T>G
XM_006720419.1:c.-8+12649T>G	XP_006720482.1:n.-8+12649T>G
XM_011521313.1:c.-8+12649T>G	XP_011519615.1:n.-8+12649T>G
XM_011521314.1:c.-8+12649T>G	XP_011519616.1:n.-8+12649T>G
NM_001369268.1:c.-8+12649T>G MANE Select	NP_001356197.1:n.-8+12649T>G
NM_001135.4:c.-8+12649T>G	NP_001126.3:n.-8+12649T>G
NM_013227.4:c.-8+12649T>G	NP_037359.3:n.-8+12649T>G