Canonical Allele Identifier: CA347266164

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73828433G>C (hg19) ; chr2:g.73601306G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73601306G>C , CM000664.2:g.73601306G>C	GRCh38
NC_000002.11:g.73828433G>C , CM000664.1:g.73828433G>C	GRCh37
NC_000002.10:g.73681941G>C	NCBI36
NG_011690.1:g.220554G>C , LRG_741:g.220554G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.11603G>C	ENSP00000507671.1:p.Arg3868Thr
ENST00000682801.1:c.11167-879G>C	ENSP00000507862.1:n.11167-879G>C
ENST00000682859.1:c.11603G>C	ENSP00000508222.1:p.Arg3868Thr
ENST00000683791.1:c.4689G>C
ENST00000684460.1:c.8884G>C
ENST00000684548.1:c.11603G>C	ENSP00000507421.1:p.Arg3868Thr
ENST00000684590.1:c.6050G>C	ENSP00000507376.1:p.Arg2017Thr
ENST00000684656.1:c.9068G>C
ENST00000613296.6:c.11984G>C MANE Select	ENSP00000482968.1:p.Arg3995Thr
ENST00000651057.1:c.2138G>C	ENSP00000498504.1:p.Arg713Thr
ENST00000651434.1:c.3340G>C
ENST00000651750.1:c.1260+425G>C
ENST00000652487.1:c.3155G>C
ENST00000464408.3:n.159G>C
ENST00000484298.5:c.11858G>C	ENSP00000478155.1:p.Arg3953Thr
ENST00000613296.4:c.11984G>C	ENSP00000482968.1:p.Arg3995Thr
ENST00000620466.4:n.5787G>C
NM_015120.4:c.11987G>C , LRG_741t1:c.11987G>C	NP_055935.4:p.Arg3996Thr
NM_001378454.1:c.11984G>C MANE Select	NP_001365383.1:p.Arg3995Thr