Canonical Allele Identifier: CA347282758
Community Standard Title: NM_001378454.1(ALMS1):c.5620A>T (p.Lys1874Ter)
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73452147A>T , CM000664.2:g.73452147A>T GRCh38
NC_000002.11:g.73679274A>T , CM000664.1:g.73679274A>T GRCh37
NC_000002.10:g.73532782A>T NCBI36
NG_011690.1:g.71395A>T , LRG_741:g.71395A>T

Transcript Alleles

HGVS Amino-acid Change
NM_001378454.1:c.5620A>T MANE Select NP_001365383.1:p.Lys1874Ter
ENST00000613296.6:c.5620A>T MANE Select ENSP00000482968.1:p.Lys1874Ter
NM_015120.4:c.5623A>T , LRG_741t1:c.5623A>T NP_055935.4:p.Lys1875Ter
ENST00000423048.5:c.451A>T ENSP00000399833.1:p.Lys151Ter
ENST00000484298.5:c.5494A>T ENSP00000478155.1:p.Lys1832Ter
ENST00000613296.4:c.5620A>T ENSP00000482968.1:p.Lys1874Ter
ENST00000614410.4:c.5620A>T ENSP00000479094.1:p.Lys1874Ter
ENST00000682565.1:c.5239A>T ENSP00000507671.1:p.Lys1747Ter
ENST00000682801.1:c.5239A>T ENSP00000507862.1:p.Lys1747Ter
ENST00000682859.1:c.5239A>T ENSP00000508222.1:p.Lys1747Ter
ENST00000683791.1:c.685+19856A>T
ENST00000684197.1:n.589A>T
ENST00000684460.1:c.2691A>T
ENST00000684548.1:c.5239A>T ENSP00000507421.1:p.Lys1747Ter
ENST00000684656.1:c.2691A>T