Canonical Allele Identifier: CA369289478
Community Standard Title: NM_018718.3(CEP41):c.33+2T>G
Gene: CEP41 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.130440932A>C , CM000669.2:g.130440932A>C GRCh38
NC_000007.13:g.130080773A>C , CM000669.1:g.130080773A>C GRCh37
NC_000007.12:g.129868009A>C NCBI36
NG_032164.1:g.5279T>G
NG_032164.2:g.5279T>G

Transcript Alleles

HGVS Amino-acid Change
NM_018718.3:c.33+2T>G MANE Select NP_061188.1:n.33+2T>G
ENST00000223208.10:c.33+2T>G MANE Select ENSP00000223208.4:n.33+2T>G
NM_001257158.1:c.33+2T>G NP_001244087.1:n.33+2T>G
NM_001257158.2:c.33+2T>G NP_001244087.1:n.33+2T>G
NM_001257159.1:c.33+2T>G NP_001244088.1:n.33+2T>G
NM_001257159.2:c.33+2T>G NP_001244088.1:n.33+2T>G
NM_001257160.1:c.33+2T>G NP_001244089.1:n.33+2T>G
NM_001257160.2:c.33+2T>G NP_001244089.1:n.33+2T>G
NM_018718.2:c.33+2T>G NP_061188.1:n.33+2T>G
NR_046443.1:n.277+2T>G
NR_046443.2:n.83+2T>G
ENST00000223208.9:c.33+2T>G ENSP00000223208.4:n.33+2T>G
ENST00000334451.6:n.91+2T>G
ENST00000343969.10:c.33+2T>G ENSP00000342738.6:n.33+2T>G
ENST00000343969.9:c.33+2T>G ENSP00000342738.5:n.33+2T>G
ENST00000469826.2:c.35T>G ENSP00000418712.2:p.Val12Gly
ENST00000471201.5:c.33+2T>G ENSP00000417463.1:n.33+2T>G
ENST00000471201.6:c.-42+2T>G ENSP00000417463.2:n.-42+2T>G
ENST00000477003.5:c.24+1465T>G ENSP00000420670.1:n.24+1465T>G
ENST00000477003.6:c.33+2T>G ENSP00000420670.2:n.33+2T>G
ENST00000480206.2:c.33+2T>G ENSP00000502099.1:n.33+2T>G
ENST00000484549.5:c.33+2T>G ENSP00000419078.1:n.33+2T>G
ENST00000484549.6:c.35T>G ENSP00000419078.2:p.Val12Gly
ENST00000489512.5:c.33+2T>G ENSP00000417815.1:n.33+2T>G
ENST00000495702.5:n.96+2T>G
ENST00000498527.5:n.93+2T>G
ENST00000541543.5:c.33+2T>G ENSP00000445888.1:n.33+2T>G
ENST00000541543.6:c.24+1465T>G ENSP00000445888.2:n.24+1465T>G
ENST00000616628.1:c.33+2T>G ENSP00000479252.1:n.33+2T>G
ENST00000674539.1:c.33+2T>G ENSP00000502834.1:n.33+2T>G
ENST00000674630.1:c.33+2T>G ENSP00000502521.1:n.33+2T>G
ENST00000675138.1:c.78+726T>G ENSP00000501597.1:n.78+726T>G
ENST00000675168.1:c.33+2T>G ENSP00000501563.1:n.33+2T>G
ENST00000675563.1:c.-513+2T>G ENSP00000502483.1:n.-513+2T>G
ENST00000675596.1:c.33+2T>G ENSP00000501735.1:n.33+2T>G
ENST00000675649.1:c.33+2T>G ENSP00000502385.1:n.33+2T>G
ENST00000675721.1:c.33+2T>G ENSP00000502026.1:n.33+2T>G
ENST00000675813.1:c.33+2T>G ENSP00000502785.1:n.33+2T>G
ENST00000675935.1:c.33+2T>G ENSP00000501731.1:n.33+2T>G
ENST00000675962.1:c.33+2T>G ENSP00000502478.1:n.33+2T>G
ENST00000676115.1:c.33+2T>G ENSP00000502631.1:n.33+2T>G
ENST00000676243.1:c.33+2T>G ENSP00000501717.1:n.33+2T>G
ENST00000676312.1:c.-7+101T>G ENSP00000502312.1:n.-7+101T>G
XM_011516708.1:c.78+726T>G XP_011515010.1:n.78+726T>G
XM_011516709.1:c.-187+2T>G XP_011515011.1:n.-187+2T>G
XM_011516709.3:c.-187+2T>G XP_011515011.1:n.-187+2T>G
XM_011516712.1:c.78+726T>G XP_011515014.1:n.78+726T>G