Canonical Allele Identifier: CA1260981426

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490083G= , CM000664.2:g.73490083G=	GRCh38
NC_000002.11:g.73717210G= , CM000664.1:g.73717210G=	GRCh37
NC_000002.10:g.73570718G=	NCBI36
NG_011690.1:g.109331G= , LRG_741:g.109331G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7743G=	ENSP00000507671.1:p.Met2581=
ENST00000682801.1:c.7743G=	ENSP00000507862.1:p.Met2581=
ENST00000682859.1:c.7743G=	ENSP00000508222.1:p.Met2581=
ENST00000683791.1:c.1135G=
ENST00000684460.1:c.5195G=
ENST00000684548.1:c.7743G=	ENSP00000507421.1:p.Met2581=
ENST00000684590.1:c.2190G=	ENSP00000507376.1:p.Met730=
ENST00000684656.1:c.5195G=
ENST00000613296.6:c.8124G= MANE Select	ENSP00000482968.1:p.Met2708=
ENST00000651434.1:c.896-29692G=
ENST00000423048.5:c.2955G=	ENSP00000399833.1:p.Met985=
ENST00000484298.5:c.7998G=	ENSP00000478155.1:p.Met2666=
ENST00000613296.4:c.8124G=	ENSP00000482968.1:p.Met2708=
ENST00000614410.4:c.8124G=	ENSP00000479094.1:p.Met2708=
ENST00000620466.4:n.1927G=
NM_015120.4:c.8127G= , LRG_741t1:c.8127G=	NP_055935.4:p.Met2709=
NM_001378454.1:c.8124G= MANE Select	NP_001365383.1:p.Met2708=