Canonical Allele Identifier: CA347267571
Community Standard Title: NM_001378454.1(ALMS1):c.2292C>G (p.Tyr764Ter)
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73448819C>G , CM000664.2:g.73448819C>G GRCh38
NC_000002.11:g.73675946C>G , CM000664.1:g.73675946C>G GRCh37
NC_000002.10:g.73529454C>G NCBI36
NG_011690.1:g.68067C>G , LRG_741:g.68067C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001378454.1:c.2292C>G MANE Select NP_001365383.1:p.Tyr764Ter
ENST00000613296.6:c.2292C>G MANE Select ENSP00000482968.1:p.Tyr764Ter
NM_015120.4:c.2295C>G , LRG_741t1:c.2295C>G NP_055935.4:p.Tyr765Ter
ENST00000484298.5:c.2166C>G ENSP00000478155.1:p.Tyr722Ter
ENST00000613296.4:c.2292C>G ENSP00000482968.1:p.Tyr764Ter
ENST00000614410.4:c.2292C>G ENSP00000479094.1:p.Tyr764Ter
ENST00000682565.1:c.1911C>G ENSP00000507671.1:p.Tyr637Ter
ENST00000682801.1:c.1911C>G ENSP00000507862.1:p.Tyr637Ter
ENST00000682859.1:c.1911C>G ENSP00000508222.1:p.Tyr637Ter
ENST00000683791.1:c.685+16528C>G
ENST00000684548.1:c.1911C>G ENSP00000507421.1:p.Tyr637Ter