Canonical Allele Identifier: CA427024436

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799762C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572635C>G , CM000664.2:g.73572635C>G	GRCh38
NC_000002.11:g.73799762C>G , CM000664.1:g.73799762C>G	GRCh37
NC_000002.10:g.73653270C>G	NCBI36
NG_011690.1:g.191883C>G , LRG_741:g.191883C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10377C>G	ENSP00000507671.1:p.Val3459=
ENST00000682801.1:c.10377C>G	ENSP00000507862.1:p.Val3459=
ENST00000682859.1:c.10377C>G	ENSP00000508222.1:p.Val3459=
ENST00000683791.1:c.3463C>G
ENST00000684460.1:c.7658C>G
ENST00000684548.1:c.10377C>G	ENSP00000507421.1:p.Val3459=
ENST00000684590.1:c.4824C>G	ENSP00000507376.1:p.Val1608=
ENST00000684656.1:c.7703C>G
ENST00000613296.6:c.10758C>G MANE Select	ENSP00000482968.1:p.Val3586=
ENST00000651057.1:c.912C>G	ENSP00000498504.1:p.Val304=
ENST00000651434.1:c.2114C>G
ENST00000651750.1:c.146C>G
ENST00000652487.1:c.1855C>G
ENST00000423048.5:c.4249C>G	ENSP00000399833.1:n.4249C>G
ENST00000484298.5:c.10632C>G	ENSP00000478155.1:p.Val3544=
ENST00000613296.4:c.10758C>G	ENSP00000482968.1:p.Val3586=
ENST00000614410.4:c.10758C>G	ENSP00000479094.1:p.Val3586=
ENST00000620466.4:n.4561C>G
NM_015120.4:c.10761C>G , LRG_741t1:c.10761C>G	NP_055935.4:p.Val3587=
NM_001378454.1:c.10758C>G MANE Select	NP_001365383.1:p.Val3586=