Canonical Allele Identifier: CA1260981514
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73490122A= , CM000664.2:g.73490122A= GRCh38
NC_000002.11:g.73717249A= , CM000664.1:g.73717249A= GRCh37
NC_000002.10:g.73570757A= NCBI36
NG_011690.1:g.109370A= , LRG_741:g.109370A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682565.1:c.7782A= ENSP00000507671.1:p.Arg2594=
ENST00000682801.1:c.7782A= ENSP00000507862.1:p.Arg2594=
ENST00000682859.1:c.7782A= ENSP00000508222.1:p.Arg2594=
ENST00000683791.1:c.1174A=
ENST00000684460.1:c.5234A=
ENST00000684548.1:c.7782A= ENSP00000507421.1:p.Arg2594=
ENST00000684590.1:c.2229A= ENSP00000507376.1:p.Arg743=
ENST00000684656.1:c.5234A=
ENST00000613296.6:c.8163A= MANE Select ENSP00000482968.1:p.Arg2721=
ENST00000651434.1:c.896-29653A=
ENST00000423048.5:c.2994A= ENSP00000399833.1:p.Arg998=
ENST00000484298.5:c.8037A= ENSP00000478155.1:p.Arg2679=
ENST00000613296.4:c.8163A= ENSP00000482968.1:p.Arg2721=
ENST00000614410.4:c.8163A= ENSP00000479094.1:p.Arg2721=
ENST00000620466.4:n.1966A=
NM_015120.4:c.8166A= , LRG_741t1:c.8166A= NP_055935.4:p.Arg2722=
NM_001378454.1:c.8163A= MANE Select NP_001365383.1:p.Arg2721=