Canonical Allele Identifier: CA347266815

Gene: ALMS1

Linked Data

• ClinVar Variation Id: 1060808
• ClinVar RCV Id: RCV001370285
• dbSNP Id: rs1672940448
• MyVariant Identifiers: chr2:g.73717080G>C (hg19) ; chr2:g.73489953G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489953G>C , CM000664.2:g.73489953G>C	GRCh38
NC_000002.11:g.73717080G>C , CM000664.1:g.73717080G>C	GRCh37
NC_000002.10:g.73570588G>C	NCBI36
NG_011690.1:g.109201G>C , LRG_741:g.109201G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7613G>C	ENSP00000507671.1:p.Ser2538Thr
ENST00000682801.1:c.7613G>C	ENSP00000507862.1:p.Ser2538Thr
ENST00000682859.1:c.7613G>C	ENSP00000508222.1:p.Ser2538Thr
ENST00000683791.1:c.1005G>C
ENST00000684460.1:c.5065G>C
ENST00000684548.1:c.7613G>C	ENSP00000507421.1:p.Ser2538Thr
ENST00000684590.1:c.2060G>C	ENSP00000507376.1:p.Ser687Thr
ENST00000684656.1:c.5065G>C
ENST00000613296.6:c.7994G>C MANE Select	ENSP00000482968.1:p.Ser2665Thr
ENST00000651434.1:c.896-29822G>C
ENST00000423048.5:c.2825G>C	ENSP00000399833.1:p.Ser942Thr
ENST00000484298.5:c.7868G>C	ENSP00000478155.1:p.Ser2623Thr
ENST00000613296.4:c.7994G>C	ENSP00000482968.1:p.Ser2665Thr
ENST00000614410.4:c.7994G>C	ENSP00000479094.1:p.Ser2665Thr
ENST00000620466.4:n.1797G>C
NM_015120.4:c.7997G>C , LRG_741t1:c.7997G>C	NP_055935.4:p.Ser2666Thr
NM_001378454.1:c.7994G>C MANE Select	NP_001365383.1:p.Ser2665Thr