Canonical Allele Identifier: CA1261022069

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572873A= , CM000664.2:g.73572873A=	GRCh38
NC_000002.11:g.73800000A= , CM000664.1:g.73800000A=	GRCh37
NC_000002.10:g.73653508A=	NCBI36
NG_011690.1:g.192121A= , LRG_741:g.192121A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10615A=	ENSP00000507671.1:p.Arg3539=
ENST00000682801.1:c.10615A=	ENSP00000507862.1:p.Arg3539=
ENST00000682859.1:c.10615A=	ENSP00000508222.1:p.Arg3539=
ENST00000683791.1:c.3701A=
ENST00000684460.1:c.7896A=
ENST00000684548.1:c.10615A=	ENSP00000507421.1:p.Arg3539=
ENST00000684590.1:c.5062A=	ENSP00000507376.1:p.Arg1688=
ENST00000684656.1:c.7941A=
ENST00000613296.6:c.10996A= MANE Select	ENSP00000482968.1:p.Arg3666=
ENST00000651057.1:c.1150A=	ENSP00000498504.1:p.Arg384=
ENST00000651434.1:c.2352A=
ENST00000651750.1:c.384A=
ENST00000652487.1:c.2093A=
ENST00000423048.5:c.4487A=	ENSP00000399833.1:n.4487A=
ENST00000484298.5:c.10870A=	ENSP00000478155.1:p.Arg3624=
ENST00000613296.4:c.10996A=	ENSP00000482968.1:p.Arg3666=
ENST00000614410.4:c.10996A=	ENSP00000479094.1:p.Arg3666=
ENST00000620466.4:n.4799A=
NM_015120.4:c.10999A= , LRG_741t1:c.10999A=	NP_055935.4:p.Arg3667=
NM_001378454.1:c.10996A= MANE Select	NP_001365383.1:p.Arg3666=