Canonical Allele Identifier: CA347265417

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73828333T>G (hg19) ; chr2:g.73601206T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73601206T>G , CM000664.2:g.73601206T>G	GRCh38
NC_000002.11:g.73828333T>G , CM000664.1:g.73828333T>G	GRCh37
NC_000002.10:g.73681841T>G	NCBI36
NG_011690.1:g.220454T>G , LRG_741:g.220454T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.11503T>G	ENSP00000507671.1:p.Phe3835Val
ENST00000682801.1:c.11167-979T>G	ENSP00000507862.1:n.11167-979T>G
ENST00000682859.1:c.11503T>G	ENSP00000508222.1:p.Phe3835Val
ENST00000683791.1:c.4589T>G
ENST00000684460.1:c.8784T>G
ENST00000684548.1:c.11503T>G	ENSP00000507421.1:p.Phe3835Val
ENST00000684590.1:c.5950T>G	ENSP00000507376.1:p.Phe1984Val
ENST00000684656.1:c.8968T>G
ENST00000613296.6:c.11884T>G MANE Select	ENSP00000482968.1:p.Phe3962Val
ENST00000651057.1:c.2038T>G	ENSP00000498504.1:p.Phe680Val
ENST00000651434.1:c.3240T>G
ENST00000651750.1:c.1260+325T>G
ENST00000652487.1:c.3055T>G
ENST00000464408.3:n.59T>G
ENST00000484298.5:c.11758T>G	ENSP00000478155.1:p.Phe3920Val
ENST00000613296.4:c.11884T>G	ENSP00000482968.1:p.Phe3962Val
ENST00000620466.4:n.5687T>G
NM_015120.4:c.11887T>G , LRG_741t1:c.11887T>G	NP_055935.4:p.Phe3963Val
NM_001378454.1:c.11884T>G MANE Select	NP_001365383.1:p.Phe3962Val