Canonical Allele Identifier: CA347283785

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799577C>A (hg19) ; chr2:g.73572450C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572450C>A , CM000664.2:g.73572450C>A	GRCh38
NC_000002.11:g.73799577C>A , CM000664.1:g.73799577C>A	GRCh37
NC_000002.10:g.73653085C>A	NCBI36
NG_011690.1:g.191698C>A , LRG_741:g.191698C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10192C>A	ENSP00000507671.1:p.His3398Asn
ENST00000682801.1:c.10192C>A	ENSP00000507862.1:p.His3398Asn
ENST00000682859.1:c.10192C>A	ENSP00000508222.1:p.His3398Asn
ENST00000683791.1:c.3278C>A
ENST00000684460.1:c.7473C>A
ENST00000684548.1:c.10192C>A	ENSP00000507421.1:p.His3398Asn
ENST00000684590.1:c.4639C>A	ENSP00000507376.1:p.His1547Asn
ENST00000684656.1:c.7518C>A
ENST00000613296.6:c.10573C>A MANE Select	ENSP00000482968.1:p.His3525Asn
ENST00000651057.1:c.727C>A	ENSP00000498504.1:p.His243Asn
ENST00000651434.1:c.1929C>A
ENST00000652487.1:c.1670C>A
ENST00000423048.5:c.4064C>A	ENSP00000399833.1:n.4064C>A
ENST00000484298.5:c.10447C>A	ENSP00000478155.1:p.His3483Asn
ENST00000613296.4:c.10573C>A	ENSP00000482968.1:p.His3525Asn
ENST00000614410.4:c.10573C>A	ENSP00000479094.1:p.His3525Asn
ENST00000620466.4:n.4376C>A
NM_015120.4:c.10576C>A , LRG_741t1:c.10576C>A	NP_055935.4:p.His3526Asn
NM_001378454.1:c.10573C>A MANE Select	NP_001365383.1:p.His3525Asn