Canonical Allele Identifier: CA347286092

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799907A>T (hg19) ; chr2:g.73572780A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572780A>T , CM000664.2:g.73572780A>T	GRCh38
NC_000002.11:g.73799907A>T , CM000664.1:g.73799907A>T	GRCh37
NC_000002.10:g.73653415A>T	NCBI36
NG_011690.1:g.192028A>T , LRG_741:g.192028A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10522A>T	ENSP00000507671.1:p.Ile3508Phe
ENST00000682801.1:c.10522A>T	ENSP00000507862.1:p.Ile3508Phe
ENST00000682859.1:c.10522A>T	ENSP00000508222.1:p.Ile3508Phe
ENST00000683791.1:c.3608A>T
ENST00000684460.1:c.7803A>T
ENST00000684548.1:c.10522A>T	ENSP00000507421.1:p.Ile3508Phe
ENST00000684590.1:c.4969A>T	ENSP00000507376.1:p.Ile1657Phe
ENST00000684656.1:c.7848A>T
ENST00000613296.6:c.10903A>T MANE Select	ENSP00000482968.1:p.Ile3635Phe
ENST00000651057.1:c.1057A>T	ENSP00000498504.1:p.Ile353Phe
ENST00000651434.1:c.2259A>T
ENST00000651750.1:c.291A>T
ENST00000652487.1:c.2000A>T
ENST00000423048.5:c.4394A>T	ENSP00000399833.1:n.4394A>T
ENST00000484298.5:c.10777A>T	ENSP00000478155.1:p.Ile3593Phe
ENST00000613296.4:c.10903A>T	ENSP00000482968.1:p.Ile3635Phe
ENST00000614410.4:c.10903A>T	ENSP00000479094.1:p.Ile3635Phe
ENST00000620466.4:n.4706A>T
NM_015120.4:c.10906A>T , LRG_741t1:c.10906A>T	NP_055935.4:p.Ile3636Phe
NM_001378454.1:c.10903A>T MANE Select	NP_001365383.1:p.Ile3635Phe