Canonical Allele Identifier: CA391065446

Gene: ANKRD9

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102507878G>C , CM000676.2:g.102507878G>C	GRCh38
NC_000014.8:g.102974215G>C , CM000676.1:g.102974215G>C	GRCh37
NC_000014.7:g.102043968G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_152326.4:c.12C>G MANE Select	NP_689539.1:p.Asp4Glu
ENST00000286918.9:c.12C>G MANE Select	ENSP00000286918.4:p.Asp4Glu
NM_001348651.1:c.12C>G	NP_001335580.1:p.Asp4Glu
NM_001348651.2:c.12C>G	NP_001335580.1:p.Asp4Glu
NM_001348652.1:c.12C>G	NP_001335581.1:p.Asp4Glu
NM_001348652.2:c.12C>G	NP_001335581.1:p.Asp4Glu
NM_152326.2:c.12C>G	NP_689539.1:p.Asp4Glu
NM_152326.3:c.12C>G	NP_689539.1:p.Asp4Glu
ENST00000286918.8:c.12C>G	ENSP00000286918.4:p.Asp4Glu
ENST00000557902.1:c.12C>G	ENSP00000454080.1:p.Asp4Glu
ENST00000559404.5:c.12C>G	ENSP00000453417.1:p.Asp4Glu
ENST00000559651.1:c.12C>G	ENSP00000454100.1:p.Asp4Glu
ENST00000560748.5:c.12C>G	ENSP00000453650.1:p.Asp4Glu
XM_005267310.2:c.12C>G	XP_005267367.1:p.Asp4Glu
XM_005267310.3:c.12C>G	XP_005267367.1:p.Asp4Glu
XM_005267311.2:c.12C>G	XP_005267368.1:p.Asp4Glu