Canonical Allele Identifier: CA347273455

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73491150T>G , CM000664.2:g.73491150T>G	GRCh38
NC_000002.11:g.73718277T>G , CM000664.1:g.73718277T>G	GRCh37
NC_000002.10:g.73571785T>G	NCBI36
NG_011690.1:g.110398T>G , LRG_741:g.110398T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.9191T>G MANE Select	NP_001365383.1:p.Leu3064Ter
ENST00000613296.6:c.9191T>G MANE Select	ENSP00000482968.1:p.Leu3064Ter
NM_015120.4:c.9194T>G , LRG_741t1:c.9194T>G	NP_055935.4:p.Leu3065Ter
ENST00000423048.5:c.3030+992T>G	ENSP00000399833.1:n.3030+992T>G
ENST00000484298.5:c.9065T>G	ENSP00000478155.1:p.Leu3022Ter
ENST00000613296.4:c.9191T>G	ENSP00000482968.1:p.Leu3064Ter
ENST00000614410.4:c.9191T>G	ENSP00000479094.1:p.Leu3064Ter
ENST00000620466.4:n.2994T>G
ENST00000651434.1:c.896-28625T>G
ENST00000652487.1:c.288T>G
ENST00000682565.1:c.8810T>G	ENSP00000507671.1:p.Leu2937Ter
ENST00000682801.1:c.8810T>G	ENSP00000507862.1:p.Leu2937Ter
ENST00000682859.1:c.8810T>G	ENSP00000508222.1:p.Leu2937Ter
ENST00000683791.1:c.2202T>G
ENST00000684460.1:c.6262T>G
ENST00000684548.1:c.8810T>G	ENSP00000507421.1:p.Leu2937Ter
ENST00000684590.1:c.3257T>G	ENSP00000507376.1:p.Leu1086Ter
ENST00000684656.1:c.6262T>G