Canonical Allele Identifier: CA178663704

Gene: C8orf34

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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