Canonical Allele Identifier: CA347259346
Community Standard Title: NM_001378454.1(ALMS1):c.619A>T (p.Arg207Ter)
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73419291A>T , CM000664.2:g.73419291A>T GRCh38
NC_000002.11:g.73646419A>T , CM000664.1:g.73646419A>T GRCh37
NC_000002.10:g.73499927A>T NCBI36
NG_011690.1:g.38537A>T , LRG_741:g.38537A>T

Transcript Alleles

HGVS Amino-acid Change
NM_001378454.1:c.619A>T MANE Select NP_001365383.1:p.Arg207Ter
ENST00000613296.6:c.619A>T MANE Select ENSP00000482968.1:p.Arg207Ter
NM_015120.4:c.622A>T , LRG_741t1:c.622A>T NP_055935.4:p.Arg208Ter
ENST00000484298.5:c.493A>T ENSP00000478155.1:p.Arg165Ter
ENST00000613296.4:c.619A>T ENSP00000482968.1:p.Arg207Ter
ENST00000614410.4:c.619A>T ENSP00000479094.1:p.Arg207Ter
ENST00000682565.1:c.169A>T ENSP00000507671.1:p.Arg57Ter
ENST00000682675.1:n.579A>T
ENST00000682801.1:c.169A>T ENSP00000507862.1:p.Arg57Ter
ENST00000682859.1:c.169A>T ENSP00000508222.1:p.Arg57Ter
ENST00000682889.1:n.584A>T
ENST00000684148.1:n.365A>T
ENST00000684548.1:c.169A>T ENSP00000507421.1:p.Arg57Ter