Canonical Allele Identifier: CA2838315410

Gene: C8orf34

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.68584495A>G , CM000670.2:g.68584495A>G	GRCh38
NC_000008.10:g.69496730A>G , CM000670.1:g.69496730A>G	GRCh37
NC_000008.9:g.69659284A>G	NCBI36
NG_055258.1:g.258774A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518698.6:c.1105+51346A>G MANE Select	ENSP00000427820.1:n.1105+51346A>G
ENST00000337103.8:c.772+51346A>G	ENSP00000337174.4:n.772+51346A>G
ENST00000518515.1:n.130+51346A>G
ENST00000518698.5:c.1105+51346A>G	ENSP00000427820.1:n.1105+51346A>G
ENST00000521406.5:c.*238+51346A>G	ENSP00000429081.1:n.*238+51346A>G
NM_052958.2:c.1105+51346A>G	NP_443190.2:n.1105+51346A>G
XM_011517445.1:c.1105+51346A>G	XP_011515747.1:n.1105+51346A>G
XM_011517446.1:c.1105+51346A>G	XP_011515748.1:n.1105+51346A>G
XM_011517447.1:c.1105+51346A>G	XP_011515749.1:n.1105+51346A>G
XM_011517448.1:c.976+51346A>G	XP_011515750.1:n.976+51346A>G
XM_011517449.1:c.1105+51346A>G	XP_011515751.1:n.1105+51346A>G
NM_001349476.1:c.1105+51346A>G	NP_001336405.1:n.1105+51346A>G
NM_001349477.1:c.1105+51346A>G	NP_001336406.1:n.1105+51346A>G
NM_001349478.1:c.976+51346A>G	NP_001336407.1:n.976+51346A>G
NM_001349479.1:c.976+51346A>G	NP_001336408.1:n.976+51346A>G
NM_052958.3:c.1105+51346A>G	NP_443190.2:n.1105+51346A>G
NR_146186.1:n.1745+51346A>G
NR_146187.1:n.1703+51346A>G
XM_011517449.2:c.1105+51346A>G	XP_011515751.1:n.1105+51346A>G
NM_052958.4:c.1105+51346A>G MANE Select	NP_443190.2:n.1105+51346A>G