Canonical Allele Identifier: CA347267865

Gene: ALMS1

Linked Data

• gnomAD v4: 2-73490169-C-G
• MyVariant Identifiers: chr2:g.73717296C>G (hg19) ; chr2:g.73490169C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490169C>G , CM000664.2:g.73490169C>G	GRCh38
NC_000002.11:g.73717296C>G , CM000664.1:g.73717296C>G	GRCh37
NC_000002.10:g.73570804C>G	NCBI36
NG_011690.1:g.109417C>G , LRG_741:g.109417C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7829C>G	ENSP00000507671.1:p.Thr2610Ser
ENST00000682801.1:c.7829C>G	ENSP00000507862.1:p.Thr2610Ser
ENST00000682859.1:c.7829C>G	ENSP00000508222.1:p.Thr2610Ser
ENST00000683791.1:c.1221C>G
ENST00000684460.1:c.5281C>G
ENST00000684548.1:c.7829C>G	ENSP00000507421.1:p.Thr2610Ser
ENST00000684590.1:c.2276C>G	ENSP00000507376.1:p.Thr759Ser
ENST00000684656.1:c.5281C>G
ENST00000613296.6:c.8210C>G MANE Select	ENSP00000482968.1:p.Thr2737Ser
ENST00000651434.1:c.896-29606C>G
ENST00000423048.5:c.3030+11C>G	ENSP00000399833.1:n.3030+11C>G
ENST00000484298.5:c.8084C>G	ENSP00000478155.1:p.Thr2695Ser
ENST00000613296.4:c.8210C>G	ENSP00000482968.1:p.Thr2737Ser
ENST00000614410.4:c.8210C>G	ENSP00000479094.1:p.Thr2737Ser
ENST00000620466.4:n.2013C>G
NM_015120.4:c.8213C>G , LRG_741t1:c.8213C>G	NP_055935.4:p.Thr2738Ser
NM_001378454.1:c.8210C>G MANE Select	NP_001365383.1:p.Thr2737Ser