Canonical Allele Identifier: CA347281231

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73519904A>T , CM000664.2:g.73519904A>T	GRCh38
NC_000002.11:g.73747031A>T , CM000664.1:g.73747031A>T	GRCh37
NC_000002.10:g.73600539A>T	NCBI36
NG_011690.1:g.139152A>T , LRG_741:g.139152A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.9669A>T MANE Select	NP_001365383.1:p.Glu3223Asp
ENST00000613296.6:c.9669A>T MANE Select	ENSP00000482968.1:p.Glu3223Asp
NM_015120.4:c.9672A>T , LRG_741t1:c.9672A>T	NP_055935.4:p.Glu3224Asp
ENST00000423048.5:c.3160A>T	ENSP00000399833.1:n.3160A>T
ENST00000484298.5:c.9543A>T	ENSP00000478155.1:p.Glu3181Asp
ENST00000613296.4:c.9669A>T	ENSP00000482968.1:p.Glu3223Asp
ENST00000614410.4:c.9669A>T	ENSP00000479094.1:p.Glu3223Asp
ENST00000620466.4:n.3472A>T
ENST00000651434.1:c.1025A>T
ENST00000652487.1:c.766A>T
ENST00000682565.1:c.9288A>T	ENSP00000507671.1:p.Glu3096Asp
ENST00000682801.1:c.9288A>T	ENSP00000507862.1:p.Glu3096Asp
ENST00000682859.1:c.9288A>T	ENSP00000508222.1:p.Glu3096Asp
ENST00000683791.1:c.2680A>T
ENST00000684460.1:c.6740A>T
ENST00000684548.1:c.9288A>T	ENSP00000507421.1:p.Glu3096Asp
ENST00000684590.1:c.3735A>T	ENSP00000507376.1:p.Glu1245Asp
ENST00000684656.1:c.6740A>T