Canonical Allele Identifier: CA347285996

Gene: ALMS1

Linked Data

• gnomAD v4: 2-73572756-G-A
• MyVariant Identifiers: chr2:g.73799883G>A (hg19) ; chr2:g.73572756G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572756G>A , CM000664.2:g.73572756G>A	GRCh38
NC_000002.11:g.73799883G>A , CM000664.1:g.73799883G>A	GRCh37
NC_000002.10:g.73653391G>A	NCBI36
NG_011690.1:g.192004G>A , LRG_741:g.192004G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10498G>A	ENSP00000507671.1:p.Asp3500Asn
ENST00000682801.1:c.10498G>A	ENSP00000507862.1:p.Asp3500Asn
ENST00000682859.1:c.10498G>A	ENSP00000508222.1:p.Asp3500Asn
ENST00000683791.1:c.3584G>A
ENST00000684460.1:c.7779G>A
ENST00000684548.1:c.10498G>A	ENSP00000507421.1:p.Asp3500Asn
ENST00000684590.1:c.4945G>A	ENSP00000507376.1:p.Asp1649Asn
ENST00000684656.1:c.7824G>A
ENST00000613296.6:c.10879G>A MANE Select	ENSP00000482968.1:p.Asp3627Asn
ENST00000651057.1:c.1033G>A	ENSP00000498504.1:p.Asp345Asn
ENST00000651434.1:c.2235G>A
ENST00000651750.1:c.267G>A
ENST00000652487.1:c.1976G>A
ENST00000423048.5:c.4370G>A	ENSP00000399833.1:n.4370G>A
ENST00000484298.5:c.10753G>A	ENSP00000478155.1:p.Asp3585Asn
ENST00000613296.4:c.10879G>A	ENSP00000482968.1:p.Asp3627Asn
ENST00000614410.4:c.10879G>A	ENSP00000479094.1:p.Asp3627Asn
ENST00000620466.4:n.4682G>A
NM_015120.4:c.10882G>A , LRG_741t1:c.10882G>A	NP_055935.4:p.Asp3628Asn
NM_001378454.1:c.10879G>A MANE Select	NP_001365383.1:p.Asp3627Asn