Canonical Allele Identifier: CA1261021116
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73572415A= , CM000664.2:g.73572415A= GRCh38
NC_000002.11:g.73799542A= , CM000664.1:g.73799542A= GRCh37
NC_000002.10:g.73653050A= NCBI36
NG_011690.1:g.191663A= , LRG_741:g.191663A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682565.1:c.10157A= ENSP00000507671.1:p.Asp3386=
ENST00000682801.1:c.10157A= ENSP00000507862.1:p.Asp3386=
ENST00000682859.1:c.10157A= ENSP00000508222.1:p.Asp3386=
ENST00000683791.1:c.3243A=
ENST00000684460.1:c.7438A=
ENST00000684548.1:c.10157A= ENSP00000507421.1:p.Asp3386=
ENST00000684590.1:c.4604A= ENSP00000507376.1:p.Asp1535=
ENST00000684656.1:c.7483A=
ENST00000613296.6:c.10538A= MANE Select ENSP00000482968.1:p.Asp3513=
ENST00000651057.1:c.692A= ENSP00000498504.1:p.Asp231=
ENST00000651434.1:c.1894A=
ENST00000652487.1:c.1635A=
ENST00000423048.5:c.4029A= ENSP00000399833.1:n.4029A=
ENST00000484298.5:c.10412A= ENSP00000478155.1:p.Asp3471=
ENST00000613296.4:c.10538A= ENSP00000482968.1:p.Asp3513=
ENST00000614410.4:c.10538A= ENSP00000479094.1:p.Asp3513=
ENST00000620466.4:n.4341A=
NM_015120.4:c.10541A= , LRG_741t1:c.10541A= NP_055935.4:p.Asp3514=
NM_001378454.1:c.10538A= MANE Select NP_001365383.1:p.Asp3513=