Canonical Allele Identifier: CA1261021970

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572810C= , CM000664.2:g.73572810C=	GRCh38
NC_000002.11:g.73799937C= , CM000664.1:g.73799937C=	GRCh37
NC_000002.10:g.73653445C=	NCBI36
NG_011690.1:g.192058C= , LRG_741:g.192058C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10552C=	ENSP00000507671.1:p.Gln3518=
ENST00000682801.1:c.10552C=	ENSP00000507862.1:p.Gln3518=
ENST00000682859.1:c.10552C=	ENSP00000508222.1:p.Gln3518=
ENST00000683791.1:c.3638C=
ENST00000684460.1:c.7833C=
ENST00000684548.1:c.10552C=	ENSP00000507421.1:p.Gln3518=
ENST00000684590.1:c.4999C=	ENSP00000507376.1:p.Gln1667=
ENST00000684656.1:c.7878C=
ENST00000613296.6:c.10933C= MANE Select	ENSP00000482968.1:p.Gln3645=
ENST00000651057.1:c.1087C=	ENSP00000498504.1:p.Gln363=
ENST00000651434.1:c.2289C=
ENST00000651750.1:c.321C=
ENST00000652487.1:c.2030C=
ENST00000423048.5:c.4424C=	ENSP00000399833.1:n.4424C=
ENST00000484298.5:c.10807C=	ENSP00000478155.1:p.Gln3603=
ENST00000613296.4:c.10933C=	ENSP00000482968.1:p.Gln3645=
ENST00000614410.4:c.10933C=	ENSP00000479094.1:p.Gln3645=
ENST00000620466.4:n.4736C=
NM_015120.4:c.10936C= , LRG_741t1:c.10936C=	NP_055935.4:p.Gln3646=
NM_001378454.1:c.10933C= MANE Select	NP_001365383.1:p.Gln3645=