Canonical Allele Identifier: CA1713322
Community Standard Title: NM_001378454.1(ALMS1):c.2309C>T (p.Pro770Leu)
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73448836C>T , CM000664.2:g.73448836C>T GRCh38
NC_000002.11:g.73675963C>T , CM000664.1:g.73675963C>T GRCh37
NC_000002.10:g.73529471C>T NCBI36
NG_011690.1:g.68084C>T , LRG_741:g.68084C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001378454.1:c.2309C>T MANE Select NP_001365383.1:p.Pro770Leu
ENST00000613296.6:c.2309C>T MANE Select ENSP00000482968.1:p.Pro770Leu
NM_015120.4:c.2312C>T , LRG_741t1:c.2312C>T NP_055935.4:p.Pro771Leu
ENST00000484298.5:c.2183C>T ENSP00000478155.1:p.Pro728Leu
ENST00000613296.4:c.2309C>T ENSP00000482968.1:p.Pro770Leu
ENST00000614410.4:c.2309C>T ENSP00000479094.1:p.Pro770Leu
ENST00000682565.1:c.1928C>T ENSP00000507671.1:p.Pro643Leu
ENST00000682801.1:c.1928C>T ENSP00000507862.1:p.Pro643Leu
ENST00000682859.1:c.1928C>T ENSP00000508222.1:p.Pro643Leu
ENST00000683791.1:c.685+16545C>T
ENST00000684548.1:c.1928C>T ENSP00000507421.1:p.Pro643Leu