Canonical Allele Identifier: CA347286427

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799958G>C (hg19) ; chr2:g.73572831G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572831G>C , CM000664.2:g.73572831G>C	GRCh38
NC_000002.11:g.73799958G>C , CM000664.1:g.73799958G>C	GRCh37
NC_000002.10:g.73653466G>C	NCBI36
NG_011690.1:g.192079G>C , LRG_741:g.192079G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10573G>C	ENSP00000507671.1:p.Asp3525His
ENST00000682801.1:c.10573G>C	ENSP00000507862.1:p.Asp3525His
ENST00000682859.1:c.10573G>C	ENSP00000508222.1:p.Asp3525His
ENST00000683791.1:c.3659G>C
ENST00000684460.1:c.7854G>C
ENST00000684548.1:c.10573G>C	ENSP00000507421.1:p.Asp3525His
ENST00000684590.1:c.5020G>C	ENSP00000507376.1:p.Asp1674His
ENST00000684656.1:c.7899G>C
ENST00000613296.6:c.10954G>C MANE Select	ENSP00000482968.1:p.Asp3652His
ENST00000651057.1:c.1108G>C	ENSP00000498504.1:p.Asp370His
ENST00000651434.1:c.2310G>C
ENST00000651750.1:c.342G>C
ENST00000652487.1:c.2051G>C
ENST00000423048.5:c.4445G>C	ENSP00000399833.1:n.4445G>C
ENST00000484298.5:c.10828G>C	ENSP00000478155.1:p.Asp3610His
ENST00000613296.4:c.10954G>C	ENSP00000482968.1:p.Asp3652His
ENST00000614410.4:c.10954G>C	ENSP00000479094.1:p.Asp3652His
ENST00000620466.4:n.4757G>C
NM_015120.4:c.10957G>C , LRG_741t1:c.10957G>C	NP_055935.4:p.Asp3653His
NM_001378454.1:c.10954G>C MANE Select	NP_001365383.1:p.Asp3652His