Canonical Allele Identifier: CA1714441

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490258A>G , CM000664.2:g.73490258A>G	GRCh38
NC_000002.11:g.73717385A>G , CM000664.1:g.73717385A>G	GRCh37
NC_000002.10:g.73570893A>G	NCBI36
NG_011690.1:g.109506A>G , LRG_741:g.109506A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.8299A>G MANE Select	NP_001365383.1:p.Lys2767Glu
ENST00000613296.6:c.8299A>G MANE Select	ENSP00000482968.1:p.Lys2767Glu
NM_015120.4:c.8302A>G , LRG_741t1:c.8302A>G	NP_055935.4:p.Lys2768Glu
ENST00000423048.5:c.3030+100A>G	ENSP00000399833.1:n.3030+100A>G
ENST00000484298.5:c.8173A>G	ENSP00000478155.1:p.Lys2725Glu
ENST00000613296.4:c.8299A>G	ENSP00000482968.1:p.Lys2767Glu
ENST00000614410.4:c.8299A>G	ENSP00000479094.1:p.Lys2767Glu
ENST00000620466.4:n.2102A>G
ENST00000651434.1:c.896-29517A>G
ENST00000682565.1:c.7918A>G	ENSP00000507671.1:p.Lys2640Glu
ENST00000682801.1:c.7918A>G	ENSP00000507862.1:p.Lys2640Glu
ENST00000682859.1:c.7918A>G	ENSP00000508222.1:p.Lys2640Glu
ENST00000683791.1:c.1310A>G
ENST00000684460.1:c.5370A>G
ENST00000684548.1:c.7918A>G	ENSP00000507421.1:p.Lys2640Glu
ENST00000684590.1:c.2365A>G	ENSP00000507376.1:p.Lys789Glu
ENST00000684656.1:c.5370A>G