Canonical Allele Identifier: CA17077882

Gene: CEP104

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3833621A>C , CM000663.2:g.3833621A>C	GRCh38
NC_000001.10:g.3750185A>C , CM000663.1:g.3750185A>C	GRCh37
NC_000001.9:g.3740045A>C	NCBI36
NG_046726.1:g.28613T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014704.4:c.1659+241T>G MANE Select	NP_055519.1:n.1659+241T>G
ENST00000378230.8:c.1659+241T>G MANE Select	ENSP00000367476.3:n.1659+241T>G
NM_014704.3:c.1659+241T>G	NP_055519.1:n.1659+241T>G
ENST00000378230.7:c.1659+241T>G	ENSP00000367476.3:n.1659+241T>G
ENST00000428079.6:c.1659+241T>G	ENSP00000394989.2:n.1659+241T>G
ENST00000438539.6:n.706+241T>G
ENST00000460038.5:n.564+241T>G
ENST00000461667.2:c.1659+241T>G	ENSP00000463605.2:n.1659+241T>G
ENST00000674544.1:c.1485+241T>G	ENSP00000502641.1:n.1485+241T>G
ENST00000674558.1:c.1659+241T>G	ENSP00000501829.1:n.1659+241T>G
ENST00000674623.1:c.1659+241T>G	ENSP00000501733.1:n.1659+241T>G
ENST00000674879.1:n.2595+241T>G
ENST00000674985.1:c.*517+241T>G	ENSP00000502482.1:n.*517+241T>G
ENST00000675108.1:c.*1575+241T>G	ENSP00000502131.1:n.*1575+241T>G
ENST00000675200.1:c.1485+241T>G	ENSP00000502512.1:n.1485+241T>G
ENST00000675334.1:n.1463+241T>G
ENST00000675375.1:c.1485+241T>G	ENSP00000502180.1:n.1485+241T>G
ENST00000675666.1:c.1659+241T>G	ENSP00000502548.1:n.1659+241T>G
ENST00000675677.1:c.1461+241T>G	ENSP00000501944.1:n.1461+241T>G
ENST00000675750.1:c.*988+241T>G	ENSP00000502342.1:n.*988+241T>G
ENST00000675966.1:n.3331+241T>G
ENST00000676009.1:c.1659+241T>G	ENSP00000502246.1:n.1659+241T>G
ENST00000676052.1:c.1677+241T>G	ENSP00000502793.1:n.1677+241T>G
XM_005244815.3:c.1767+241T>G	XP_005244872.1:n.1767+241T>G
XM_005244815.4:c.1767+241T>G	XP_005244872.1:n.1767+241T>G
XM_011542473.1:c.1785+241T>G	XP_011540775.1:n.1785+241T>G
XM_011542474.1:c.1677+241T>G	XP_011540776.1:n.1677+241T>G
XM_011542474.3:c.1677+241T>G	XP_011540776.1:n.1677+241T>G
XM_011542475.1:c.1611+241T>G	XP_011540777.1:n.1611+241T>G
XM_011542476.1:c.1587+241T>G	XP_011540778.1:n.1587+241T>G
XM_011542477.1:c.1413+241T>G	XP_011540779.1:n.1413+241T>G
XM_011542478.1:c.1785+241T>G	XP_011540780.1:n.1785+241T>G
XM_017002918.2:c.1485+241T>G	XP_016858407.1:n.1485+241T>G
XM_017002919.2:c.1461+241T>G	XP_016858408.1:n.1461+241T>G
XM_024451101.1:c.1785+241T>G	XP_024306869.1:n.1785+241T>G
XM_024451102.1:c.1611+241T>G	XP_024306870.1:n.1611+241T>G
XM_024451103.1:c.1593+241T>G	XP_024306871.1:n.1593+241T>G
XM_024451104.1:c.1587+241T>G	XP_024306872.1:n.1587+241T>G
XM_024451106.1:c.1413+241T>G	XP_024306874.1:n.1413+241T>G
XM_024451108.1:c.1785+241T>G	XP_024306876.1:n.1785+241T>G