Canonical Allele Identifier: CA1261033845
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73601311T= , CM000664.2:g.73601311T= GRCh38
NC_000002.11:g.73828438T= , CM000664.1:g.73828438T= GRCh37
NC_000002.10:g.73681946T= NCBI36
NG_011690.1:g.220559T= , LRG_741:g.220559T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682565.1:c.11608T= ENSP00000507671.1:p.Trp3870=
ENST00000682801.1:c.11167-874T= ENSP00000507862.1:n.11167-874T=
ENST00000682859.1:c.11608T= ENSP00000508222.1:p.Trp3870=
ENST00000683791.1:c.4694T=
ENST00000684460.1:c.8889T=
ENST00000684548.1:c.11608T= ENSP00000507421.1:p.Trp3870=
ENST00000684590.1:c.6055T= ENSP00000507376.1:p.Trp2019=
ENST00000684656.1:c.9073T=
ENST00000613296.6:c.11989T= MANE Select ENSP00000482968.1:p.Trp3997=
ENST00000651057.1:c.2143T= ENSP00000498504.1:p.Trp715=
ENST00000651434.1:c.3345T=
ENST00000651750.1:c.1260+430T=
ENST00000652487.1:c.3160T=
ENST00000464408.3:n.164T=
ENST00000484298.5:c.11863T= ENSP00000478155.1:p.Trp3955=
ENST00000613296.4:c.11989T= ENSP00000482968.1:p.Trp3997=
ENST00000620466.4:n.5792T=
NM_015120.4:c.11992T= , LRG_741t1:c.11992T= NP_055935.4:p.Trp3998=
NM_001378454.1:c.11989T= MANE Select NP_001365383.1:p.Trp3997=