Canonical Allele Identifier: CA347260650
Community Standard Title: NM_001378454.1(ALMS1):c.857C>G (p.Ser286Ter)
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73424522C>G , CM000664.2:g.73424522C>G GRCh38
NC_000002.11:g.73651650C>G , CM000664.1:g.73651650C>G GRCh37
NC_000002.10:g.73505158C>G NCBI36
NG_011690.1:g.43768C>G , LRG_741:g.43768C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001378454.1:c.857C>G MANE Select NP_001365383.1:p.Ser286Ter
ENST00000613296.6:c.857C>G MANE Select ENSP00000482968.1:p.Ser286Ter
NM_015120.4:c.860C>G , LRG_741t1:c.860C>G NP_055935.4:p.Ser287Ter
ENST00000484298.5:c.731C>G ENSP00000478155.1:p.Ser244Ter
ENST00000613296.4:c.857C>G ENSP00000482968.1:p.Ser286Ter
ENST00000614410.4:c.857C>G ENSP00000479094.1:p.Ser286Ter
ENST00000682565.1:c.407C>G ENSP00000507671.1:p.Ser136Ter
ENST00000682675.1:n.817C>G
ENST00000682801.1:c.407C>G ENSP00000507862.1:p.Ser136Ter
ENST00000682859.1:c.407C>G ENSP00000508222.1:p.Ser136Ter
ENST00000682889.1:n.822C>G
ENST00000683791.1:c.211C>G
ENST00000684548.1:c.407C>G ENSP00000507421.1:p.Ser136Ter