Canonical Allele Identifier: CA1260981311
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73490033A= , CM000664.2:g.73490033A= GRCh38
NC_000002.11:g.73717160A= , CM000664.1:g.73717160A= GRCh37
NC_000002.10:g.73570668A= NCBI36
NG_011690.1:g.109281A= , LRG_741:g.109281A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682565.1:c.7693A= ENSP00000507671.1:p.Lys2565=
ENST00000682801.1:c.7693A= ENSP00000507862.1:p.Lys2565=
ENST00000682859.1:c.7693A= ENSP00000508222.1:p.Lys2565=
ENST00000683791.1:c.1085A=
ENST00000684460.1:c.5145A=
ENST00000684548.1:c.7693A= ENSP00000507421.1:p.Lys2565=
ENST00000684590.1:c.2140A= ENSP00000507376.1:p.Lys714=
ENST00000684656.1:c.5145A=
ENST00000613296.6:c.8074A= MANE Select ENSP00000482968.1:p.Lys2692=
ENST00000651434.1:c.896-29742A=
ENST00000423048.5:c.2905A= ENSP00000399833.1:p.Lys969=
ENST00000484298.5:c.7948A= ENSP00000478155.1:p.Lys2650=
ENST00000613296.4:c.8074A= ENSP00000482968.1:p.Lys2692=
ENST00000614410.4:c.8074A= ENSP00000479094.1:p.Lys2692=
ENST00000620466.4:n.1877A=
NM_015120.4:c.8077A= , LRG_741t1:c.8077A= NP_055935.4:p.Lys2693=
NM_001378454.1:c.8074A= MANE Select NP_001365383.1:p.Lys2692=