Canonical Allele Identifier: CA1260981479

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490102A= , CM000664.2:g.73490102A=	GRCh38
NC_000002.11:g.73717229A= , CM000664.1:g.73717229A=	GRCh37
NC_000002.10:g.73570737A=	NCBI36
NG_011690.1:g.109350A= , LRG_741:g.109350A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7762A=	ENSP00000507671.1:p.Ile2588=
ENST00000682801.1:c.7762A=	ENSP00000507862.1:p.Ile2588=
ENST00000682859.1:c.7762A=	ENSP00000508222.1:p.Ile2588=
ENST00000683791.1:c.1154A=
ENST00000684460.1:c.5214A=
ENST00000684548.1:c.7762A=	ENSP00000507421.1:p.Ile2588=
ENST00000684590.1:c.2209A=	ENSP00000507376.1:p.Ile737=
ENST00000684656.1:c.5214A=
ENST00000613296.6:c.8143A= MANE Select	ENSP00000482968.1:p.Ile2715=
ENST00000651434.1:c.896-29673A=
ENST00000423048.5:c.2974A=	ENSP00000399833.1:p.Ile992=
ENST00000484298.5:c.8017A=	ENSP00000478155.1:p.Ile2673=
ENST00000613296.4:c.8143A=	ENSP00000482968.1:p.Ile2715=
ENST00000614410.4:c.8143A=	ENSP00000479094.1:p.Ile2715=
ENST00000620466.4:n.1946A=
NM_015120.4:c.8146A= , LRG_741t1:c.8146A=	NP_055935.4:p.Ile2716=
NM_001378454.1:c.8143A= MANE Select	NP_001365383.1:p.Ile2715=