Canonical Allele Identifier: CA347283549

Gene: ALMS1

Linked Data

• dbSNP Id: rs1674950307
• gnomAD v3: 2-73572424-A-G
• gnomAD v4: 2-73572424-A-G
• MyVariant Identifiers: chr2:g.73799551A>G (hg19) ; chr2:g.73572424A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572424A>G , CM000664.2:g.73572424A>G	GRCh38
NC_000002.11:g.73799551A>G , CM000664.1:g.73799551A>G	GRCh37
NC_000002.10:g.73653059A>G	NCBI36
NG_011690.1:g.191672A>G , LRG_741:g.191672A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10166A>G	ENSP00000507671.1:p.Gln3389Arg
ENST00000682801.1:c.10166A>G	ENSP00000507862.1:p.Gln3389Arg
ENST00000682859.1:c.10166A>G	ENSP00000508222.1:p.Gln3389Arg
ENST00000683791.1:c.3252A>G
ENST00000684460.1:c.7447A>G
ENST00000684548.1:c.10166A>G	ENSP00000507421.1:p.Gln3389Arg
ENST00000684590.1:c.4613A>G	ENSP00000507376.1:p.Gln1538Arg
ENST00000684656.1:c.7492A>G
ENST00000613296.6:c.10547A>G MANE Select	ENSP00000482968.1:p.Gln3516Arg
ENST00000651057.1:c.701A>G	ENSP00000498504.1:p.Gln234Arg
ENST00000651434.1:c.1903A>G
ENST00000652487.1:c.1644A>G
ENST00000423048.5:c.4038A>G	ENSP00000399833.1:n.4038A>G
ENST00000484298.5:c.10421A>G	ENSP00000478155.1:p.Gln3474Arg
ENST00000613296.4:c.10547A>G	ENSP00000482968.1:p.Gln3516Arg
ENST00000614410.4:c.10547A>G	ENSP00000479094.1:p.Gln3516Arg
ENST00000620466.4:n.4350A>G
NM_015120.4:c.10550A>G , LRG_741t1:c.10550A>G	NP_055935.4:p.Gln3517Arg
NM_001378454.1:c.10547A>G MANE Select	NP_001365383.1:p.Gln3516Arg