Canonical Allele Identifier: CA347279189
Community Standard Title: NM_001378454.1(ALMS1):c.4751C>G (p.Ala1584Gly)
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73451278C>G , CM000664.2:g.73451278C>G GRCh38
NC_000002.11:g.73678405C>G , CM000664.1:g.73678405C>G GRCh37
NC_000002.10:g.73531913C>G NCBI36
NG_011690.1:g.70526C>G , LRG_741:g.70526C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001378454.1:c.4751C>G MANE Select NP_001365383.1:p.Ala1584Gly
ENST00000613296.6:c.4751C>G MANE Select ENSP00000482968.1:p.Ala1584Gly
NM_015120.4:c.4754C>G , LRG_741t1:c.4754C>G NP_055935.4:p.Ala1585Gly
ENST00000484298.5:c.4625C>G ENSP00000478155.1:p.Ala1542Gly
ENST00000613296.4:c.4751C>G ENSP00000482968.1:p.Ala1584Gly
ENST00000614410.4:c.4751C>G ENSP00000479094.1:p.Ala1584Gly
ENST00000682565.1:c.4370C>G ENSP00000507671.1:p.Ala1457Gly
ENST00000682801.1:c.4370C>G ENSP00000507862.1:p.Ala1457Gly
ENST00000682859.1:c.4370C>G ENSP00000508222.1:p.Ala1457Gly
ENST00000683791.1:c.685+18987C>G
ENST00000684460.1:c.1822C>G
ENST00000684548.1:c.4370C>G ENSP00000507421.1:p.Ala1457Gly
ENST00000684656.1:c.1822C>G