Canonical Allele Identifier: CA1715027
Gene: ALMS1 HGNC NCBI

Linked Data

dbSNP Id: rs555485864
gnomAD v2: 2-73799574-G-A
gnomAD v3: 2-73572447-G-A
gnomAD v4: 2-73572447-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73572447G>A , CM000664.2:g.73572447G>A GRCh38
NC_000002.11:g.73799574G>A , CM000664.1:g.73799574G>A GRCh37
NC_000002.10:g.73653082G>A NCBI36
NG_011690.1:g.191695G>A , LRG_741:g.191695G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682565.1:c.10189G>A ENSP00000507671.1:p.Glu3397Lys
ENST00000682801.1:c.10189G>A ENSP00000507862.1:p.Glu3397Lys
ENST00000682859.1:c.10189G>A ENSP00000508222.1:p.Glu3397Lys
ENST00000683791.1:c.3275G>A
ENST00000684460.1:c.7470G>A
ENST00000684548.1:c.10189G>A ENSP00000507421.1:p.Glu3397Lys
ENST00000684590.1:c.4636G>A ENSP00000507376.1:p.Glu1546Lys
ENST00000684656.1:c.7515G>A
ENST00000613296.6:c.10570G>A MANE Select ENSP00000482968.1:p.Glu3524Lys
ENST00000651057.1:c.724G>A ENSP00000498504.1:p.Glu242Lys
ENST00000651434.1:c.1926G>A
ENST00000652487.1:c.1667G>A
ENST00000423048.5:c.4061G>A ENSP00000399833.1:n.4061G>A
ENST00000484298.5:c.10444G>A ENSP00000478155.1:p.Glu3482Lys
ENST00000613296.4:c.10570G>A ENSP00000482968.1:p.Glu3524Lys
ENST00000614410.4:c.10570G>A ENSP00000479094.1:p.Glu3524Lys
ENST00000620466.4:n.4373G>A
NM_015120.4:c.10573G>A , LRG_741t1:c.10573G>A NP_055935.4:p.Glu3525Lys
NM_001378454.1:c.10570G>A MANE Select NP_001365383.1:p.Glu3524Lys