Canonical Allele Identifier: CA426783616

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73828521T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73601394T>G , CM000664.2:g.73601394T>G	GRCh38
NC_000002.11:g.73828521T>G , CM000664.1:g.73828521T>G	GRCh37
NC_000002.10:g.73682029T>G	NCBI36
NG_011690.1:g.220642T>G , LRG_741:g.220642T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.11691T>G	ENSP00000507671.1:p.Ala3897=
ENST00000682801.1:c.11167-791T>G	ENSP00000507862.1:n.11167-791T>G
ENST00000682859.1:c.11691T>G	ENSP00000508222.1:p.Ala3897=
ENST00000683791.1:c.4777T>G
ENST00000684460.1:c.8972T>G
ENST00000684548.1:c.11691T>G	ENSP00000507421.1:p.Ala3897=
ENST00000684590.1:c.6138T>G	ENSP00000507376.1:p.Ala2046=
ENST00000684656.1:c.9156T>G
ENST00000613296.6:c.12072T>G MANE Select	ENSP00000482968.1:p.Ala4024=
ENST00000651057.1:c.2226T>G	ENSP00000498504.1:p.Ala742=
ENST00000651434.1:c.3428T>G
ENST00000651750.1:c.1260+513T>G
ENST00000652487.1:c.3243T>G
ENST00000464408.3:n.247T>G
ENST00000484298.5:c.11946T>G	ENSP00000478155.1:p.Ala3982=
ENST00000613296.4:c.12072T>G	ENSP00000482968.1:p.Ala4024=
ENST00000620466.4:n.5875T>G
NM_015120.4:c.12075T>G , LRG_741t1:c.12075T>G	NP_055935.4:p.Ala4025=
NM_001378454.1:c.12072T>G MANE Select	NP_001365383.1:p.Ala4024=