Canonical Allele Identifier: CA1261021233

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572485C= , CM000664.2:g.73572485C=	GRCh38
NC_000002.11:g.73799612C= , CM000664.1:g.73799612C=	GRCh37
NC_000002.10:g.73653120C=	NCBI36
NG_011690.1:g.191733C= , LRG_741:g.191733C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10227C=	ENSP00000507671.1:p.Asp3409=
ENST00000682801.1:c.10227C=	ENSP00000507862.1:p.Asp3409=
ENST00000682859.1:c.10227C=	ENSP00000508222.1:p.Asp3409=
ENST00000683791.1:c.3313C=
ENST00000684460.1:c.7508C=
ENST00000684548.1:c.10227C=	ENSP00000507421.1:p.Asp3409=
ENST00000684590.1:c.4674C=	ENSP00000507376.1:p.Asp1558=
ENST00000684656.1:c.7553C=
ENST00000613296.6:c.10608C= MANE Select	ENSP00000482968.1:p.Asp3536=
ENST00000651057.1:c.762C=	ENSP00000498504.1:p.Asp254=
ENST00000651434.1:c.1964C=
ENST00000652487.1:c.1705C=
ENST00000423048.5:c.4099C=	ENSP00000399833.1:n.4099C=
ENST00000484298.5:c.10482C=	ENSP00000478155.1:p.Asp3494=
ENST00000613296.4:c.10608C=	ENSP00000482968.1:p.Asp3536=
ENST00000614410.4:c.10608C=	ENSP00000479094.1:p.Asp3536=
ENST00000620466.4:n.4411C=
NM_015120.4:c.10611C= , LRG_741t1:c.10611C=	NP_055935.4:p.Asp3537=
NM_001378454.1:c.10608C= MANE Select	NP_001365383.1:p.Asp3536=