Canonical Allele Identifier: CA347273596
Community Standard Title: NM_001378454.1(ALMS1):c.3050G>A (p.Trp1017Ter)
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73449577G>A , CM000664.2:g.73449577G>A GRCh38
NC_000002.11:g.73676704G>A , CM000664.1:g.73676704G>A GRCh37
NC_000002.10:g.73530212G>A NCBI36
NG_011690.1:g.68825G>A , LRG_741:g.68825G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001378454.1:c.3050G>A MANE Select NP_001365383.1:p.Trp1017Ter
ENST00000613296.6:c.3050G>A MANE Select ENSP00000482968.1:p.Trp1017Ter
NM_015120.4:c.3053G>A , LRG_741t1:c.3053G>A NP_055935.4:p.Trp1018Ter
ENST00000484298.5:c.2924G>A ENSP00000478155.1:p.Trp975Ter
ENST00000613296.4:c.3050G>A ENSP00000482968.1:p.Trp1017Ter
ENST00000614410.4:c.3050G>A ENSP00000479094.1:p.Trp1017Ter
ENST00000682565.1:c.2669G>A ENSP00000507671.1:p.Trp890Ter
ENST00000682801.1:c.2669G>A ENSP00000507862.1:p.Trp890Ter
ENST00000682859.1:c.2669G>A ENSP00000508222.1:p.Trp890Ter
ENST00000683791.1:c.685+17286G>A
ENST00000684460.1:c.121G>A
ENST00000684548.1:c.2669G>A ENSP00000507421.1:p.Trp890Ter
ENST00000684656.1:c.121G>A