Canonical Allele Identifier: CA347286141

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799916A>G (hg19) ; chr2:g.73572789A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572789A>G , CM000664.2:g.73572789A>G	GRCh38
NC_000002.11:g.73799916A>G , CM000664.1:g.73799916A>G	GRCh37
NC_000002.10:g.73653424A>G	NCBI36
NG_011690.1:g.192037A>G , LRG_741:g.192037A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10531A>G	ENSP00000507671.1:p.Asn3511Asp
ENST00000682801.1:c.10531A>G	ENSP00000507862.1:p.Asn3511Asp
ENST00000682859.1:c.10531A>G	ENSP00000508222.1:p.Asn3511Asp
ENST00000683791.1:c.3617A>G
ENST00000684460.1:c.7812A>G
ENST00000684548.1:c.10531A>G	ENSP00000507421.1:p.Asn3511Asp
ENST00000684590.1:c.4978A>G	ENSP00000507376.1:p.Asn1660Asp
ENST00000684656.1:c.7857A>G
ENST00000613296.6:c.10912A>G MANE Select	ENSP00000482968.1:p.Asn3638Asp
ENST00000651057.1:c.1066A>G	ENSP00000498504.1:p.Asn356Asp
ENST00000651434.1:c.2268A>G
ENST00000651750.1:c.300A>G
ENST00000652487.1:c.2009A>G
ENST00000423048.5:c.4403A>G	ENSP00000399833.1:n.4403A>G
ENST00000484298.5:c.10786A>G	ENSP00000478155.1:p.Asn3596Asp
ENST00000613296.4:c.10912A>G	ENSP00000482968.1:p.Asn3638Asp
ENST00000614410.4:c.10912A>G	ENSP00000479094.1:p.Asn3638Asp
ENST00000620466.4:n.4715A>G
NM_015120.4:c.10915A>G , LRG_741t1:c.10915A>G	NP_055935.4:p.Asn3639Asp
NM_001378454.1:c.10912A>G MANE Select	NP_001365383.1:p.Asn3638Asp