Canonical Allele Identifier: CA347286692

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799993G>C (hg19) ; chr2:g.73572866G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572866G>C , CM000664.2:g.73572866G>C	GRCh38
NC_000002.11:g.73799993G>C , CM000664.1:g.73799993G>C	GRCh37
NC_000002.10:g.73653501G>C	NCBI36
NG_011690.1:g.192114G>C , LRG_741:g.192114G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10608G>C	ENSP00000507671.1:p.Trp3536Cys
ENST00000682801.1:c.10608G>C	ENSP00000507862.1:p.Trp3536Cys
ENST00000682859.1:c.10608G>C	ENSP00000508222.1:p.Trp3536Cys
ENST00000683791.1:c.3694G>C
ENST00000684460.1:c.7889G>C
ENST00000684548.1:c.10608G>C	ENSP00000507421.1:p.Trp3536Cys
ENST00000684590.1:c.5055G>C	ENSP00000507376.1:p.Trp1685Cys
ENST00000684656.1:c.7934G>C
ENST00000613296.6:c.10989G>C MANE Select	ENSP00000482968.1:p.Trp3663Cys
ENST00000651057.1:c.1143G>C	ENSP00000498504.1:p.Trp381Cys
ENST00000651434.1:c.2345G>C
ENST00000651750.1:c.377G>C
ENST00000652487.1:c.2086G>C
ENST00000423048.5:c.4480G>C	ENSP00000399833.1:n.4480G>C
ENST00000484298.5:c.10863G>C	ENSP00000478155.1:p.Trp3621Cys
ENST00000613296.4:c.10989G>C	ENSP00000482968.1:p.Trp3663Cys
ENST00000614410.4:c.10989G>C	ENSP00000479094.1:p.Trp3663Cys
ENST00000620466.4:n.4792G>C
NM_015120.4:c.10992G>C , LRG_741t1:c.10992G>C	NP_055935.4:p.Trp3664Cys
NM_001378454.1:c.10989G>C MANE Select	NP_001365383.1:p.Trp3663Cys