Canonical Allele Identifier: CA347273936
Community Standard Title: NM_001378454.1(ALMS1):c.3136C>T (p.Gln1046Ter)
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73449663C>T , CM000664.2:g.73449663C>T GRCh38
NC_000002.11:g.73676790C>T , CM000664.1:g.73676790C>T GRCh37
NC_000002.10:g.73530298C>T NCBI36
NG_011690.1:g.68911C>T , LRG_741:g.68911C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001378454.1:c.3136C>T MANE Select NP_001365383.1:p.Gln1046Ter
ENST00000613296.6:c.3136C>T MANE Select ENSP00000482968.1:p.Gln1046Ter
NM_015120.4:c.3139C>T , LRG_741t1:c.3139C>T NP_055935.4:p.Gln1047Ter
ENST00000484298.5:c.3010C>T ENSP00000478155.1:p.Gln1004Ter
ENST00000613296.4:c.3136C>T ENSP00000482968.1:p.Gln1046Ter
ENST00000614410.4:c.3136C>T ENSP00000479094.1:p.Gln1046Ter
ENST00000682565.1:c.2755C>T ENSP00000507671.1:p.Gln919Ter
ENST00000682801.1:c.2755C>T ENSP00000507862.1:p.Gln919Ter
ENST00000682859.1:c.2755C>T ENSP00000508222.1:p.Gln919Ter
ENST00000683791.1:c.685+17372C>T
ENST00000684460.1:c.207C>T
ENST00000684548.1:c.2755C>T ENSP00000507421.1:p.Gln919Ter
ENST00000684656.1:c.207C>T