Canonical Allele Identifier: CA1713884

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73451974A>G , CM000664.2:g.73451974A>G	GRCh38
NC_000002.11:g.73679101A>G , CM000664.1:g.73679101A>G	GRCh37
NC_000002.10:g.73532609A>G	NCBI36
NG_011690.1:g.71222A>G , LRG_741:g.71222A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.5447A>G MANE Select	NP_001365383.1:p.Tyr1816Cys
ENST00000613296.6:c.5447A>G MANE Select	ENSP00000482968.1:p.Tyr1816Cys
NM_015120.4:c.5450A>G , LRG_741t1:c.5450A>G	NP_055935.4:p.Tyr1817Cys
ENST00000423048.5:c.278A>G	ENSP00000399833.1:p.Tyr93Cys
ENST00000484298.5:c.5321A>G	ENSP00000478155.1:p.Tyr1774Cys
ENST00000613296.4:c.5447A>G	ENSP00000482968.1:p.Tyr1816Cys
ENST00000614410.4:c.5447A>G	ENSP00000479094.1:p.Tyr1816Cys
ENST00000682565.1:c.5066A>G	ENSP00000507671.1:p.Tyr1689Cys
ENST00000682801.1:c.5066A>G	ENSP00000507862.1:p.Tyr1689Cys
ENST00000682859.1:c.5066A>G	ENSP00000508222.1:p.Tyr1689Cys
ENST00000683791.1:c.685+19683A>G
ENST00000684197.1:n.416A>G
ENST00000684460.1:c.2518A>G
ENST00000684548.1:c.5066A>G	ENSP00000507421.1:p.Tyr1689Cys
ENST00000684656.1:c.2518A>G