Canonical Allele Identifier: CA1743237267

Gene: CEP41

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.130395299T= , CM000669.2:g.130395299T=	GRCh38
NC_000007.13:g.130035140T= , CM000669.1:g.130035140T=	GRCh37
NC_000007.12:g.129822376T=	NCBI36
NG_032164.1:g.50912A=
NG_032164.2:g.50912A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000223208.10:c.*3592A= MANE Select	ENSP00000223208.4:n.*3592A=
ENST00000541543.6:c.*3592A=	ENSP00000445888.2:n.*3592A=
ENST00000675649.1:c.*3592A=	ENSP00000502385.1:n.*3592A=
ENST00000223208.9:c.*3592A=	ENSP00000223208.4:n.*3592A=
ENST00000541543.5:c.*3592A=	ENSP00000445888.1:n.*3592A=
NM_001257158.1:c.*3592A=	NP_001244087.1:n.*3592A=
NM_001257159.1:c.*3592A=	NP_001244088.1:n.*3592A=
NM_018718.2:c.*3592A=	NP_061188.1:n.*3592A=
NR_046443.1:n.4882A=
NM_018718.3:c.*3592A= MANE Select	NP_061188.1:n.*3592A=
NM_001257158.2:c.*3592A=	NP_001244087.1:n.*3592A=
NR_046443.2:n.4688A=
NM_001257159.2:c.*3592A=	NP_001244088.1:n.*3592A=