Canonical Allele Identifier: CA347286748

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73800001G>C (hg19) ; chr2:g.73572874G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572874G>C , CM000664.2:g.73572874G>C	GRCh38
NC_000002.11:g.73800001G>C , CM000664.1:g.73800001G>C	GRCh37
NC_000002.10:g.73653509G>C	NCBI36
NG_011690.1:g.192122G>C , LRG_741:g.192122G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10616G>C	ENSP00000507671.1:p.Arg3539Thr
ENST00000682801.1:c.10616G>C	ENSP00000507862.1:p.Arg3539Thr
ENST00000682859.1:c.10616G>C	ENSP00000508222.1:p.Arg3539Thr
ENST00000683791.1:c.3702G>C
ENST00000684460.1:c.7897G>C
ENST00000684548.1:c.10616G>C	ENSP00000507421.1:p.Arg3539Thr
ENST00000684590.1:c.5063G>C	ENSP00000507376.1:p.Arg1688Thr
ENST00000684656.1:c.7942G>C
ENST00000613296.6:c.10997G>C MANE Select	ENSP00000482968.1:p.Arg3666Thr
ENST00000651057.1:c.1151G>C	ENSP00000498504.1:p.Arg384Thr
ENST00000651434.1:c.2353G>C
ENST00000651750.1:c.385G>C
ENST00000652487.1:c.2094G>C
ENST00000423048.5:c.4488G>C	ENSP00000399833.1:n.4488G>C
ENST00000484298.5:c.10871G>C	ENSP00000478155.1:p.Arg3624Thr
ENST00000613296.4:c.10997G>C	ENSP00000482968.1:p.Arg3666Thr
ENST00000614410.4:c.10997G>C	ENSP00000479094.1:p.Arg3666Thr
ENST00000620466.4:n.4800G>C
NM_015120.4:c.11000G>C , LRG_741t1:c.11000G>C	NP_055935.4:p.Arg3667Thr
NM_001378454.1:c.10997G>C MANE Select	NP_001365383.1:p.Arg3666Thr