Canonical Allele Identifier: CA347278116
Community Standard Title: NM_001378454.1(ALMS1):c.4321C>T (p.Gln1441Ter)
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73450848C>T , CM000664.2:g.73450848C>T GRCh38
NC_000002.11:g.73677975C>T , CM000664.1:g.73677975C>T GRCh37
NC_000002.10:g.73531483C>T NCBI36
NG_011690.1:g.70096C>T , LRG_741:g.70096C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001378454.1:c.4321C>T MANE Select NP_001365383.1:p.Gln1441Ter
ENST00000613296.6:c.4321C>T MANE Select ENSP00000482968.1:p.Gln1441Ter
NM_015120.4:c.4324C>T , LRG_741t1:c.4324C>T NP_055935.4:p.Gln1442Ter
ENST00000484298.5:c.4195C>T ENSP00000478155.1:p.Gln1399Ter
ENST00000613296.4:c.4321C>T ENSP00000482968.1:p.Gln1441Ter
ENST00000614410.4:c.4321C>T ENSP00000479094.1:p.Gln1441Ter
ENST00000682565.1:c.3940C>T ENSP00000507671.1:p.Gln1314Ter
ENST00000682801.1:c.3940C>T ENSP00000507862.1:p.Gln1314Ter
ENST00000682859.1:c.3940C>T ENSP00000508222.1:p.Gln1314Ter
ENST00000683791.1:c.685+18557C>T
ENST00000684460.1:c.1392C>T
ENST00000684548.1:c.3940C>T ENSP00000507421.1:p.Gln1314Ter
ENST00000684656.1:c.1392C>T