Canonical Allele Identifier: CA1713325
Community Standard Title: NM_001378454.1(ALMS1):c.2326C>T (p.Gln776Ter)
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73448853C>T , CM000664.2:g.73448853C>T GRCh38
NC_000002.11:g.73675980C>T , CM000664.1:g.73675980C>T GRCh37
NC_000002.10:g.73529488C>T NCBI36
NG_011690.1:g.68101C>T , LRG_741:g.68101C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001378454.1:c.2326C>T MANE Select NP_001365383.1:p.Gln776Ter
ENST00000613296.6:c.2326C>T MANE Select ENSP00000482968.1:p.Gln776Ter
NM_015120.4:c.2329C>T , LRG_741t1:c.2329C>T NP_055935.4:p.Gln777Ter
ENST00000484298.5:c.2200C>T ENSP00000478155.1:p.Gln734Ter
ENST00000613296.4:c.2326C>T ENSP00000482968.1:p.Gln776Ter
ENST00000614410.4:c.2326C>T ENSP00000479094.1:p.Gln776Ter
ENST00000682565.1:c.1945C>T ENSP00000507671.1:p.Gln649Ter
ENST00000682801.1:c.1945C>T ENSP00000507862.1:p.Gln649Ter
ENST00000682859.1:c.1945C>T ENSP00000508222.1:p.Gln649Ter
ENST00000683791.1:c.685+16562C>T
ENST00000684548.1:c.1945C>T ENSP00000507421.1:p.Gln649Ter