Canonical Allele Identifier: CA427024586

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799825G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572698G>A , CM000664.2:g.73572698G>A	GRCh38
NC_000002.11:g.73799825G>A , CM000664.1:g.73799825G>A	GRCh37
NC_000002.10:g.73653333G>A	NCBI36
NG_011690.1:g.191946G>A , LRG_741:g.191946G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10440G>A	ENSP00000507671.1:p.Glu3480=
ENST00000682801.1:c.10440G>A	ENSP00000507862.1:p.Glu3480=
ENST00000682859.1:c.10440G>A	ENSP00000508222.1:p.Glu3480=
ENST00000683791.1:c.3526G>A
ENST00000684460.1:c.7721G>A
ENST00000684548.1:c.10440G>A	ENSP00000507421.1:p.Glu3480=
ENST00000684590.1:c.4887G>A	ENSP00000507376.1:p.Glu1629=
ENST00000684656.1:c.7766G>A
ENST00000613296.6:c.10821G>A MANE Select	ENSP00000482968.1:p.Glu3607=
ENST00000651057.1:c.975G>A	ENSP00000498504.1:p.Glu325=
ENST00000651434.1:c.2177G>A
ENST00000651750.1:c.209G>A
ENST00000652487.1:c.1918G>A
ENST00000423048.5:c.4312G>A	ENSP00000399833.1:n.4312G>A
ENST00000484298.5:c.10695G>A	ENSP00000478155.1:p.Glu3565=
ENST00000613296.4:c.10821G>A	ENSP00000482968.1:p.Glu3607=
ENST00000614410.4:c.10821G>A	ENSP00000479094.1:p.Glu3607=
ENST00000620466.4:n.4624G>A
NM_015120.4:c.10824G>A , LRG_741t1:c.10824G>A	NP_055935.4:p.Glu3608=
NM_001378454.1:c.10821G>A MANE Select	NP_001365383.1:p.Glu3607=