Canonical Allele Identifier: CA1261021762

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572732G= , CM000664.2:g.73572732G=	GRCh38
NC_000002.11:g.73799859G= , CM000664.1:g.73799859G=	GRCh37
NC_000002.10:g.73653367G=	NCBI36
NG_011690.1:g.191980G= , LRG_741:g.191980G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10474G=	ENSP00000507671.1:p.Asp3492=
ENST00000682801.1:c.10474G=	ENSP00000507862.1:p.Asp3492=
ENST00000682859.1:c.10474G=	ENSP00000508222.1:p.Asp3492=
ENST00000683791.1:c.3560G=
ENST00000684460.1:c.7755G=
ENST00000684548.1:c.10474G=	ENSP00000507421.1:p.Asp3492=
ENST00000684590.1:c.4921G=	ENSP00000507376.1:p.Asp1641=
ENST00000684656.1:c.7800G=
ENST00000613296.6:c.10855G= MANE Select	ENSP00000482968.1:p.Asp3619=
ENST00000651057.1:c.1009G=	ENSP00000498504.1:p.Asp337=
ENST00000651434.1:c.2211G=
ENST00000651750.1:c.243G=
ENST00000652487.1:c.1952G=
ENST00000423048.5:c.4346G=	ENSP00000399833.1:n.4346G=
ENST00000484298.5:c.10729G=	ENSP00000478155.1:p.Asp3577=
ENST00000613296.4:c.10855G=	ENSP00000482968.1:p.Asp3619=
ENST00000614410.4:c.10855G=	ENSP00000479094.1:p.Asp3619=
ENST00000620466.4:n.4658G=
NM_015120.4:c.10858G= , LRG_741t1:c.10858G=	NP_055935.4:p.Asp3620=
NM_001378454.1:c.10855G= MANE Select	NP_001365383.1:p.Asp3619=