Canonical Allele Identifier: CA347261872
Community Standard Title: NM_001378454.1(ALMS1):c.1266C>A (p.Asp422Glu)
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73426481C>A , CM000664.2:g.73426481C>A GRCh38
NC_000002.11:g.73653609C>A , CM000664.1:g.73653609C>A GRCh37
NC_000002.10:g.73507117C>A NCBI36
NG_011690.1:g.45727C>A , LRG_741:g.45727C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001378454.1:c.1266C>A MANE Select NP_001365383.1:p.Asp422Glu
ENST00000613296.6:c.1266C>A MANE Select ENSP00000482968.1:p.Asp422Glu
NM_015120.4:c.1269C>A , LRG_741t1:c.1269C>A NP_055935.4:p.Asp423Glu
ENST00000484298.5:c.1140C>A ENSP00000478155.1:p.Asp380Glu
ENST00000613296.4:c.1266C>A ENSP00000482968.1:p.Asp422Glu
ENST00000614410.4:c.1266C>A ENSP00000479094.1:p.Asp422Glu
ENST00000682565.1:c.816C>A ENSP00000507671.1:p.Asp272Glu
ENST00000682801.1:c.816C>A ENSP00000507862.1:p.Asp272Glu
ENST00000682859.1:c.816C>A ENSP00000508222.1:p.Asp272Glu
ENST00000682889.1:n.1231C>A
ENST00000683791.1:c.591+1579C>A
ENST00000684548.1:c.816C>A ENSP00000507421.1:p.Asp272Glu