Canonical Allele Identifier: CA1715068

Gene: ALMS1

Linked Data

• dbSNP Id: rs767806649
• ExAC: 2:73799834 G / A
• gnomAD v2: 2-73799834-G-A
• gnomAD v4: 2-73572707-G-A
• MyVariant Identifiers: chr2:g.73799834G>A (hg19) ; chr2:g.73572707G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572707G>A , CM000664.2:g.73572707G>A	GRCh38
NC_000002.11:g.73799834G>A , CM000664.1:g.73799834G>A	GRCh37
NC_000002.10:g.73653342G>A	NCBI36
NG_011690.1:g.191955G>A , LRG_741:g.191955G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10449G>A	ENSP00000507671.1:p.Arg3483=
ENST00000682801.1:c.10449G>A	ENSP00000507862.1:p.Arg3483=
ENST00000682859.1:c.10449G>A	ENSP00000508222.1:p.Arg3483=
ENST00000683791.1:c.3535G>A
ENST00000684460.1:c.7730G>A
ENST00000684548.1:c.10449G>A	ENSP00000507421.1:p.Arg3483=
ENST00000684590.1:c.4896G>A	ENSP00000507376.1:p.Arg1632=
ENST00000684656.1:c.7775G>A
ENST00000613296.6:c.10830G>A MANE Select	ENSP00000482968.1:p.Arg3610=
ENST00000651057.1:c.984G>A	ENSP00000498504.1:p.Arg328=
ENST00000651434.1:c.2186G>A
ENST00000651750.1:c.218G>A
ENST00000652487.1:c.1927G>A
ENST00000423048.5:c.4321G>A	ENSP00000399833.1:n.4321G>A
ENST00000484298.5:c.10704G>A	ENSP00000478155.1:p.Arg3568=
ENST00000613296.4:c.10830G>A	ENSP00000482968.1:p.Arg3610=
ENST00000614410.4:c.10830G>A	ENSP00000479094.1:p.Arg3610=
ENST00000620466.4:n.4633G>A
NM_015120.4:c.10833G>A , LRG_741t1:c.10833G>A	NP_055935.4:p.Arg3611=
NM_001378454.1:c.10830G>A MANE Select	NP_001365383.1:p.Arg3610=