Canonical Allele Identifier: CA1713150

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73432279C>A , CM000664.2:g.73432279C>A	GRCh38
NC_000002.11:g.73659407C>A , CM000664.1:g.73659407C>A	GRCh37
NC_000002.10:g.73512915C>A	NCBI36
NG_011690.1:g.51525C>A , LRG_741:g.51525C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.1420C>A MANE Select	NP_001365383.1:p.His474Asn
ENST00000613296.6:c.1420C>A MANE Select	ENSP00000482968.1:p.His474Asn
NM_015120.4:c.1423C>A , LRG_741t1:c.1423C>A	NP_055935.4:p.His475Asn
ENST00000484298.5:c.1294C>A	ENSP00000478155.1:p.His432Asn
ENST00000613296.4:c.1420C>A	ENSP00000482968.1:p.His474Asn
ENST00000614410.4:c.1420C>A	ENSP00000479094.1:p.His474Asn
ENST00000682565.1:c.1039C>A	ENSP00000507671.1:p.His347Asn
ENST00000682801.1:c.1039C>A	ENSP00000507862.1:p.His347Asn
ENST00000682859.1:c.1039C>A	ENSP00000508222.1:p.His347Asn
ENST00000682889.1:n.1385C>A
ENST00000683791.1:c.673C>A
ENST00000684548.1:c.1039C>A	ENSP00000507421.1:p.His347Asn