Canonical Allele Identifier: CA1261034060
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73601404_73601408delinsCTACT , CM000664.2:g.73601404_73601408delinsCTACT GRCh38
NC_000002.11:g.73828531_73828535delinsCTACT , CM000664.1:g.73828531_73828535delinsCTACT GRCh37
NC_000002.10:g.73682039_73682043delinsCTACT NCBI36
NG_011690.1:g.220652_220656delinsCTACT , LRG_741:g.220652_220656delinsCTACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000682565.1:c.11701_11705delinsCTACT ENSP00000507671.1:p.Leu3901=
ENST00000682801.1:c.11167-781_11167-777delinsCTACT ENSP00000507862.1:n.11167-781_11167-777delinsCTACT
ENST00000682859.1:c.11701_11705delinsCTACT ENSP00000508222.1:p.Leu3901=
ENST00000683791.1:c.4787_4791delinsCTACT
ENST00000684460.1:c.8982_8986delinsCTACT
ENST00000684548.1:c.11701_11705delinsCTACT ENSP00000507421.1:p.Leu3901=
ENST00000684590.1:c.6148_6152delinsCTACT ENSP00000507376.1:p.Leu2050=
ENST00000684656.1:c.9166_9170delinsCTACT
ENST00000613296.6:c.12082_12086delinsCTACT MANE Select ENSP00000482968.1:p.Leu4028=
ENST00000651057.1:c.2236_2240delinsCTACT ENSP00000498504.1:p.Leu746=
ENST00000651434.1:c.3438_3442delinsCTACT
ENST00000651750.1:c.1260+523_1260+527delinsCTACT
ENST00000652487.1:c.3253_3257delinsCTACT
ENST00000464408.3:n.257_261delinsCTACT
ENST00000484298.5:c.11956_11960delinsCTACT ENSP00000478155.1:p.Leu3986=
ENST00000613296.4:c.12082_12086delinsCTACT ENSP00000482968.1:p.Leu4028=
ENST00000620466.4:n.5885_5889delinsCTACT
NM_015120.4:c.12085_12089delinsCTACT , LRG_741t1:c.12085_12089delinsCTACT NP_055935.4:p.Leu4029=
NM_001378454.1:c.12082_12086delinsCTACT MANE Select NP_001365383.1:p.Leu4028=