Canonical Allele Identifier: CA1261021905

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572772T= , CM000664.2:g.73572772T=	GRCh38
NC_000002.11:g.73799899T= , CM000664.1:g.73799899T=	GRCh37
NC_000002.10:g.73653407T=	NCBI36
NG_011690.1:g.192020T= , LRG_741:g.192020T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10514T=	ENSP00000507671.1:p.Leu3505=
ENST00000682801.1:c.10514T=	ENSP00000507862.1:p.Leu3505=
ENST00000682859.1:c.10514T=	ENSP00000508222.1:p.Leu3505=
ENST00000683791.1:c.3600T=
ENST00000684460.1:c.7795T=
ENST00000684548.1:c.10514T=	ENSP00000507421.1:p.Leu3505=
ENST00000684590.1:c.4961T=	ENSP00000507376.1:p.Leu1654=
ENST00000684656.1:c.7840T=
ENST00000613296.6:c.10895T= MANE Select	ENSP00000482968.1:p.Leu3632=
ENST00000651057.1:c.1049T=	ENSP00000498504.1:p.Leu350=
ENST00000651434.1:c.2251T=
ENST00000651750.1:c.283T=
ENST00000652487.1:c.1992T=
ENST00000423048.5:c.4386T=	ENSP00000399833.1:n.4386T=
ENST00000484298.5:c.10769T=	ENSP00000478155.1:p.Leu3590=
ENST00000613296.4:c.10895T=	ENSP00000482968.1:p.Leu3632=
ENST00000614410.4:c.10895T=	ENSP00000479094.1:p.Leu3632=
ENST00000620466.4:n.4698T=
NM_015120.4:c.10898T= , LRG_741t1:c.10898T=	NP_055935.4:p.Leu3633=
NM_001378454.1:c.10895T= MANE Select	NP_001365383.1:p.Leu3632=