Canonical Allele Identifier: CA50392119

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73449576T>A , CM000664.2:g.73449576T>A	GRCh38
NC_000002.11:g.73676703T>A , CM000664.1:g.73676703T>A	GRCh37
NC_000002.10:g.73530211T>A	NCBI36
NG_011690.1:g.68824T>A , LRG_741:g.68824T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.3049T>A MANE Select	NP_001365383.1:p.Trp1017Arg
ENST00000613296.6:c.3049T>A MANE Select	ENSP00000482968.1:p.Trp1017Arg
NM_015120.4:c.3052T>A , LRG_741t1:c.3052T>A	NP_055935.4:p.Trp1018Arg
ENST00000484298.5:c.2923T>A	ENSP00000478155.1:p.Trp975Arg
ENST00000613296.4:c.3049T>A	ENSP00000482968.1:p.Trp1017Arg
ENST00000614410.4:c.3049T>A	ENSP00000479094.1:p.Trp1017Arg
ENST00000682565.1:c.2668T>A	ENSP00000507671.1:p.Trp890Arg
ENST00000682801.1:c.2668T>A	ENSP00000507862.1:p.Trp890Arg
ENST00000682859.1:c.2668T>A	ENSP00000508222.1:p.Trp890Arg
ENST00000683791.1:c.685+17285T>A
ENST00000684460.1:c.120T>A
ENST00000684548.1:c.2668T>A	ENSP00000507421.1:p.Trp890Arg
ENST00000684656.1:c.120T>A