Canonical Allele Identifier: CA1261033503

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73601106C= , CM000664.2:g.73601106C=	GRCh38
NC_000002.11:g.73828233C= , CM000664.1:g.73828233C=	GRCh37
NC_000002.10:g.73681741C=	NCBI36
NG_011690.1:g.220354C= , LRG_741:g.220354C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.11492-89C=	ENSP00000507671.1:n.11492-89C=
ENST00000682801.1:c.11167-1079C=	ENSP00000507862.1:n.11167-1079C=
ENST00000682859.1:c.11492-89C=	ENSP00000508222.1:n.11492-89C=
ENST00000683791.1:c.4578-89C=
ENST00000684460.1:c.8773-89C=
ENST00000684548.1:c.11492-89C=	ENSP00000507421.1:n.11492-89C=
ENST00000684590.1:c.5939-89C=	ENSP00000507376.1:n.5939-89C=
ENST00000684656.1:c.8957-89C=
ENST00000613296.6:c.11873-89C= MANE Select	ENSP00000482968.1:n.11873-89C=
ENST00000651057.1:c.2027-89C=	ENSP00000498504.1:n.2027-89C=
ENST00000651434.1:c.3229-89C=
ENST00000651750.1:c.1260+225C=
ENST00000652487.1:c.3044-89C=
ENST00000464408.3:n.48-89C=
ENST00000484298.5:c.11747-89C=	ENSP00000478155.1:n.11747-89C=
ENST00000613296.4:c.11873-89C=	ENSP00000482968.1:n.11873-89C=
ENST00000620466.4:n.5676-89C=
NM_015120.4:c.11876-89C= , LRG_741t1:c.11876-89C=	NP_055935.4:n.11876-89C=
NM_001378454.1:c.11873-89C= MANE Select	NP_001365383.1:n.11873-89C=