Canonical Allele Identifier: CA347286459

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799962A>C (hg19) ; chr2:g.73572835A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572835A>C , CM000664.2:g.73572835A>C	GRCh38
NC_000002.11:g.73799962A>C , CM000664.1:g.73799962A>C	GRCh37
NC_000002.10:g.73653470A>C	NCBI36
NG_011690.1:g.192083A>C , LRG_741:g.192083A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10577A>C	ENSP00000507671.1:p.Asp3526Ala
ENST00000682801.1:c.10577A>C	ENSP00000507862.1:p.Asp3526Ala
ENST00000682859.1:c.10577A>C	ENSP00000508222.1:p.Asp3526Ala
ENST00000683791.1:c.3663A>C
ENST00000684460.1:c.7858A>C
ENST00000684548.1:c.10577A>C	ENSP00000507421.1:p.Asp3526Ala
ENST00000684590.1:c.5024A>C	ENSP00000507376.1:p.Asp1675Ala
ENST00000684656.1:c.7903A>C
ENST00000613296.6:c.10958A>C MANE Select	ENSP00000482968.1:p.Asp3653Ala
ENST00000651057.1:c.1112A>C	ENSP00000498504.1:p.Asp371Ala
ENST00000651434.1:c.2314A>C
ENST00000651750.1:c.346A>C
ENST00000652487.1:c.2055A>C
ENST00000423048.5:c.4449A>C	ENSP00000399833.1:n.4449A>C
ENST00000484298.5:c.10832A>C	ENSP00000478155.1:p.Asp3611Ala
ENST00000613296.4:c.10958A>C	ENSP00000482968.1:p.Asp3653Ala
ENST00000614410.4:c.10958A>C	ENSP00000479094.1:p.Asp3653Ala
ENST00000620466.4:n.4761A>C
NM_015120.4:c.10961A>C , LRG_741t1:c.10961A>C	NP_055935.4:p.Asp3654Ala
NM_001378454.1:c.10958A>C MANE Select	NP_001365383.1:p.Asp3653Ala