Canonical Allele Identifier: CA347263830

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73716762G>C (hg19) ; chr2:g.73489635G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489635G>C , CM000664.2:g.73489635G>C	GRCh38
NC_000002.11:g.73716762G>C , CM000664.1:g.73716762G>C	GRCh37
NC_000002.10:g.73570270G>C	NCBI36
NG_011690.1:g.108883G>C , LRG_741:g.108883G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7295G>C	ENSP00000507671.1:p.Gly2432Ala
ENST00000682801.1:c.7295G>C	ENSP00000507862.1:p.Gly2432Ala
ENST00000682859.1:c.7295G>C	ENSP00000508222.1:p.Gly2432Ala
ENST00000683791.1:c.687G>C
ENST00000684460.1:c.4747G>C
ENST00000684548.1:c.7295G>C	ENSP00000507421.1:p.Gly2432Ala
ENST00000684590.1:c.1742G>C	ENSP00000507376.1:p.Gly581Ala
ENST00000684656.1:c.4747G>C
ENST00000613296.6:c.7676G>C MANE Select	ENSP00000482968.1:p.Gly2559Ala
ENST00000651434.1:c.896-30140G>C
ENST00000423048.5:c.2507G>C	ENSP00000399833.1:p.Gly836Ala
ENST00000484298.5:c.7550G>C	ENSP00000478155.1:p.Gly2517Ala
ENST00000613296.4:c.7676G>C	ENSP00000482968.1:p.Gly2559Ala
ENST00000614410.4:c.7676G>C	ENSP00000479094.1:p.Gly2559Ala
ENST00000620466.4:n.1479G>C
NM_015120.4:c.7679G>C , LRG_741t1:c.7679G>C	NP_055935.4:p.Gly2560Ala
NM_001378454.1:c.7676G>C MANE Select	NP_001365383.1:p.Gly2559Ala