Canonical Allele Identifier: CA1713335
Community Standard Title: NM_001378454.1(ALMS1):c.2396A>G (p.Gln799Arg)
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73448923A>G , CM000664.2:g.73448923A>G GRCh38
NC_000002.11:g.73676050A>G , CM000664.1:g.73676050A>G GRCh37
NC_000002.10:g.73529558A>G NCBI36
NG_011690.1:g.68171A>G , LRG_741:g.68171A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001378454.1:c.2396A>G MANE Select NP_001365383.1:p.Gln799Arg
ENST00000613296.6:c.2396A>G MANE Select ENSP00000482968.1:p.Gln799Arg
NM_015120.4:c.2399A>G , LRG_741t1:c.2399A>G NP_055935.4:p.Gln800Arg
ENST00000484298.5:c.2270A>G ENSP00000478155.1:p.Gln757Arg
ENST00000613296.4:c.2396A>G ENSP00000482968.1:p.Gln799Arg
ENST00000614410.4:c.2396A>G ENSP00000479094.1:p.Gln799Arg
ENST00000682565.1:c.2015A>G ENSP00000507671.1:p.Gln672Arg
ENST00000682801.1:c.2015A>G ENSP00000507862.1:p.Gln672Arg
ENST00000682859.1:c.2015A>G ENSP00000508222.1:p.Gln672Arg
ENST00000683791.1:c.685+16632A>G
ENST00000684548.1:c.2015A>G ENSP00000507421.1:p.Gln672Arg