Canonical Allele Identifier: CA347262021
Community Standard Title: NM_001378454.1(ALMS1):c.1336A>T (p.Lys446Ter)
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73426551A>T , CM000664.2:g.73426551A>T GRCh38
NC_000002.11:g.73653679A>T , CM000664.1:g.73653679A>T GRCh37
NC_000002.10:g.73507187A>T NCBI36
NG_011690.1:g.45797A>T , LRG_741:g.45797A>T

Transcript Alleles

HGVS Amino-acid Change
NM_001378454.1:c.1336A>T MANE Select NP_001365383.1:p.Lys446Ter
ENST00000613296.6:c.1336A>T MANE Select ENSP00000482968.1:p.Lys446Ter
NM_015120.4:c.1339A>T , LRG_741t1:c.1339A>T NP_055935.4:p.Lys447Ter
ENST00000484298.5:c.1210A>T ENSP00000478155.1:p.Lys404Ter
ENST00000613296.4:c.1336A>T ENSP00000482968.1:p.Lys446Ter
ENST00000614410.4:c.1336A>T ENSP00000479094.1:p.Lys446Ter
ENST00000682565.1:c.886A>T ENSP00000507671.1:p.Lys296Ter
ENST00000682801.1:c.886A>T ENSP00000507862.1:p.Lys296Ter
ENST00000682859.1:c.886A>T ENSP00000508222.1:p.Lys296Ter
ENST00000682889.1:n.1301A>T
ENST00000683791.1:c.591+1649A>T
ENST00000684548.1:c.886A>T ENSP00000507421.1:p.Lys296Ter