Canonical Allele Identifier: CA347266789

Gene: ALMS1

Linked Data

• gnomAD v4: 2-73601377-G-C
• MyVariant Identifiers: chr2:g.73828504G>C (hg19) ; chr2:g.73601377G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73601377G>C , CM000664.2:g.73601377G>C	GRCh38
NC_000002.11:g.73828504G>C , CM000664.1:g.73828504G>C	GRCh37
NC_000002.10:g.73682012G>C	NCBI36
NG_011690.1:g.220625G>C , LRG_741:g.220625G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.11674G>C	ENSP00000507671.1:p.Gly3892Arg
ENST00000682801.1:c.11167-808G>C	ENSP00000507862.1:n.11167-808G>C
ENST00000682859.1:c.11674G>C	ENSP00000508222.1:p.Gly3892Arg
ENST00000683791.1:c.4760G>C
ENST00000684460.1:c.8955G>C
ENST00000684548.1:c.11674G>C	ENSP00000507421.1:p.Gly3892Arg
ENST00000684590.1:c.6121G>C	ENSP00000507376.1:p.Gly2041Arg
ENST00000684656.1:c.9139G>C
ENST00000613296.6:c.12055G>C MANE Select	ENSP00000482968.1:p.Gly4019Arg
ENST00000651057.1:c.2209G>C	ENSP00000498504.1:p.Gly737Arg
ENST00000651434.1:c.3411G>C
ENST00000651750.1:c.1260+496G>C
ENST00000652487.1:c.3226G>C
ENST00000464408.3:n.230G>C
ENST00000484298.5:c.11929G>C	ENSP00000478155.1:p.Gly3977Arg
ENST00000613296.4:c.12055G>C	ENSP00000482968.1:p.Gly4019Arg
ENST00000620466.4:n.5858G>C
NM_015120.4:c.12058G>C , LRG_741t1:c.12058G>C	NP_055935.4:p.Gly4020Arg
NM_001378454.1:c.12055G>C MANE Select	NP_001365383.1:p.Gly4019Arg