Canonical Allele Identifier: CA582620740
Gene: C8orf34 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.68476982C>A , CM000670.2:g.68476982C>A GRCh38
NC_000008.10:g.69389217C>A , CM000670.1:g.69389217C>A GRCh37
NC_000008.9:g.69551771C>A NCBI36
NG_055258.1:g.151261C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000518698.6:c.736+8162C>A MANE Select ENSP00000427820.1:n.736+8162C>A
ENST00000337103.8:c.403+8162C>A ENSP00000337174.4:n.403+8162C>A
ENST00000348340.6:c.478+8162C>A ENSP00000345255.2:n.478+8162C>A
ENST00000349492.3:n.479-11041C>A
ENST00000518698.5:c.736+8162C>A ENSP00000427820.1:n.736+8162C>A
ENST00000521406.5:c.403+8162C>A ENSP00000429081.1:n.403+8162C>A
NM_001195639.1:c.736+8162C>A NP_001182568.1:n.736+8162C>A
NM_052958.2:c.736+8162C>A NP_443190.2:n.736+8162C>A
XM_011517445.1:c.736+8162C>A XP_011515747.1:n.736+8162C>A
XM_011517446.1:c.736+8162C>A XP_011515748.1:n.736+8162C>A
XM_011517447.1:c.736+8162C>A XP_011515749.1:n.736+8162C>A
XM_011517448.1:c.608-11041C>A XP_011515750.1:n.608-11041C>A
XM_011517449.1:c.736+8162C>A XP_011515751.1:n.736+8162C>A
XM_011517450.1:c.736+8162C>A XP_011515752.1:n.736+8162C>A
XM_011517452.1:c.736+8162C>A XP_011515754.1:n.736+8162C>A
XR_928756.1:n.794+8162C>A
NM_001195639.2:c.736+8162C>A NP_001182568.1:n.736+8162C>A
NM_001349476.1:c.736+8162C>A NP_001336405.1:n.736+8162C>A
NM_001349477.1:c.736+8162C>A NP_001336406.1:n.736+8162C>A
NM_001349478.1:c.608-11041C>A NP_001336407.1:n.608-11041C>A
NM_001349479.1:c.608-11041C>A NP_001336408.1:n.608-11041C>A
NM_001349480.1:c.608-11041C>A NP_001336409.1:n.608-11041C>A
NM_052958.3:c.736+8162C>A NP_443190.2:n.736+8162C>A
NR_146186.1:n.1376+8162C>A
NR_146187.1:n.1248-11041C>A
XM_011517449.2:c.736+8162C>A XP_011515751.1:n.736+8162C>A
XM_011517450.2:c.736+8162C>A XP_011515752.1:n.736+8162C>A
XR_928756.3:n.999+8162C>A
NM_052958.4:c.736+8162C>A MANE Select NP_443190.2:n.736+8162C>A
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