Canonical Allele Identifier: CA347264364
Community Standard Title: NM_001378454.1(ALMS1):c.1433-2A>G
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73447958A>G , CM000664.2:g.73447958A>G GRCh38
NC_000002.11:g.73675088A>G , CM000664.1:g.73675088A>G GRCh37
NC_000002.10:g.73528596A>G NCBI36
NG_011690.1:g.67206A>G , LRG_741:g.67206A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001378454.1:c.1433-2A>G MANE Select NP_001365383.1:n.1433-2A>G
ENST00000613296.6:c.1433-2A>G MANE Select ENSP00000482968.1:n.1433-2A>G
NM_015120.4:c.1436-2A>G , LRG_741t1:c.1436-2A>G NP_055935.4:n.1436-2A>G
ENST00000484298.5:c.1307-2A>G ENSP00000478155.1:n.1307-2A>G
ENST00000613296.4:c.1433-2A>G ENSP00000482968.1:n.1433-2A>G
ENST00000614410.4:c.1433-2A>G ENSP00000479094.1:n.1433-2A>G
ENST00000682565.1:c.1052-2A>G ENSP00000507671.1:n.1052-2A>G
ENST00000682801.1:c.1052-2A>G ENSP00000507862.1:n.1052-2A>G
ENST00000682859.1:c.1052-2A>G ENSP00000508222.1:n.1052-2A>G
ENST00000683791.1:c.685+15667A>G
ENST00000684548.1:c.1052-2A>G ENSP00000507421.1:n.1052-2A>G