Canonical Allele Identifier: CA1260981272

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490006T= , CM000664.2:g.73490006T=	GRCh38
NC_000002.11:g.73717133T= , CM000664.1:g.73717133T=	GRCh37
NC_000002.10:g.73570641T=	NCBI36
NG_011690.1:g.109254T= , LRG_741:g.109254T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7666T=	ENSP00000507671.1:p.Leu2556=
ENST00000682801.1:c.7666T=	ENSP00000507862.1:p.Leu2556=
ENST00000682859.1:c.7666T=	ENSP00000508222.1:p.Leu2556=
ENST00000683791.1:c.1058T=
ENST00000684460.1:c.5118T=
ENST00000684548.1:c.7666T=	ENSP00000507421.1:p.Leu2556=
ENST00000684590.1:c.2113T=	ENSP00000507376.1:p.Leu705=
ENST00000684656.1:c.5118T=
ENST00000613296.6:c.8047T= MANE Select	ENSP00000482968.1:p.Leu2683=
ENST00000651434.1:c.896-29769T=
ENST00000423048.5:c.2878T=	ENSP00000399833.1:p.Leu960=
ENST00000484298.5:c.7921T=	ENSP00000478155.1:p.Leu2641=
ENST00000613296.4:c.8047T=	ENSP00000482968.1:p.Leu2683=
ENST00000614410.4:c.8047T=	ENSP00000479094.1:p.Leu2683=
ENST00000620466.4:n.1850T=
NM_015120.4:c.8050T= , LRG_741t1:c.8050T=	NP_055935.4:p.Leu2684=
NM_001378454.1:c.8047T= MANE Select	NP_001365383.1:p.Leu2683=