Canonical Allele Identifier: CA1743237032

Gene: CEP41

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.130395209T= , CM000669.2:g.130395209T=	GRCh38
NC_000007.13:g.130035050T= , CM000669.1:g.130035050T=	GRCh37
NC_000007.12:g.129822286T=	NCBI36
NG_032164.1:g.51002A=
NG_032164.2:g.51002A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223208.10:c.*3682A= MANE Select	ENSP00000223208.4:n.*3682A=
ENST00000541543.6:c.*3682A=	ENSP00000445888.2:n.*3682A=
ENST00000675649.1:c.*3682A=	ENSP00000502385.1:n.*3682A=
ENST00000223208.9:c.*3682A=	ENSP00000223208.4:n.*3682A=
ENST00000541543.5:c.*3682A=	ENSP00000445888.1:n.*3682A=
NM_001257158.1:c.*3682A=	NP_001244087.1:n.*3682A=
NM_001257159.1:c.*3682A=	NP_001244088.1:n.*3682A=
NM_018718.2:c.*3682A=	NP_061188.1:n.*3682A=
NR_046443.1:n.4972A=
NM_018718.3:c.*3682A= MANE Select	NP_061188.1:n.*3682A=
NM_001257158.2:c.*3682A=	NP_001244087.1:n.*3682A=
NR_046443.2:n.4778A=
NM_001257159.2:c.*3682A=	NP_001244088.1:n.*3682A=