Canonical Allele Identifier: CA1713521

Gene: ALMS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73449939A>G , CM000664.2:g.73449939A>G	GRCh38
NC_000002.11:g.73677066A>G , CM000664.1:g.73677066A>G	GRCh37
NC_000002.10:g.73530574A>G	NCBI36
NG_011690.1:g.69187A>G , LRG_741:g.69187A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.3031A>G	ENSP00000507671.1:p.Thr1011Ala
ENST00000682801.1:c.3031A>G	ENSP00000507862.1:p.Thr1011Ala
ENST00000682859.1:c.3031A>G	ENSP00000508222.1:p.Thr1011Ala
ENST00000683791.1:c.685+17648A>G
ENST00000684460.1:c.483A>G
ENST00000684548.1:c.3031A>G	ENSP00000507421.1:p.Thr1011Ala
ENST00000684656.1:c.483A>G
ENST00000613296.6:c.3412A>G MANE Select	ENSP00000482968.1:p.Thr1138Ala
ENST00000484298.5:c.3286A>G	ENSP00000478155.1:p.Thr1096Ala
ENST00000613296.4:c.3412A>G	ENSP00000482968.1:p.Thr1138Ala
ENST00000614410.4:c.3412A>G	ENSP00000479094.1:p.Thr1138Ala
NM_015120.4:c.3415A>G , LRG_741t1:c.3415A>G	NP_055935.4:p.Thr1139Ala
NM_001378454.1:c.3412A>G MANE Select	NP_001365383.1:p.Thr1138Ala