Canonical Allele Identifier: CA347286587

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799980G>C (hg19) ; chr2:g.73572853G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572853G>C , CM000664.2:g.73572853G>C	GRCh38
NC_000002.11:g.73799980G>C , CM000664.1:g.73799980G>C	GRCh37
NC_000002.10:g.73653488G>C	NCBI36
NG_011690.1:g.192101G>C , LRG_741:g.192101G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10595G>C	ENSP00000507671.1:p.Ser3532Thr
ENST00000682801.1:c.10595G>C	ENSP00000507862.1:p.Ser3532Thr
ENST00000682859.1:c.10595G>C	ENSP00000508222.1:p.Ser3532Thr
ENST00000683791.1:c.3681G>C
ENST00000684460.1:c.7876G>C
ENST00000684548.1:c.10595G>C	ENSP00000507421.1:p.Ser3532Thr
ENST00000684590.1:c.5042G>C	ENSP00000507376.1:p.Ser1681Thr
ENST00000684656.1:c.7921G>C
ENST00000613296.6:c.10976G>C MANE Select	ENSP00000482968.1:p.Ser3659Thr
ENST00000651057.1:c.1130G>C	ENSP00000498504.1:p.Ser377Thr
ENST00000651434.1:c.2332G>C
ENST00000651750.1:c.364G>C
ENST00000652487.1:c.2073G>C
ENST00000423048.5:c.4467G>C	ENSP00000399833.1:n.4467G>C
ENST00000484298.5:c.10850G>C	ENSP00000478155.1:p.Ser3617Thr
ENST00000613296.4:c.10976G>C	ENSP00000482968.1:p.Ser3659Thr
ENST00000614410.4:c.10976G>C	ENSP00000479094.1:p.Ser3659Thr
ENST00000620466.4:n.4779G>C
NM_015120.4:c.10979G>C , LRG_741t1:c.10979G>C	NP_055935.4:p.Ser3660Thr
NM_001378454.1:c.10976G>C MANE Select	NP_001365383.1:p.Ser3659Thr