Canonical Allele Identifier: CA347264181

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73716920A>G (hg19) ; chr2:g.73489793A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73489793A>G , CM000664.2:g.73489793A>G	GRCh38
NC_000002.11:g.73716920A>G , CM000664.1:g.73716920A>G	GRCh37
NC_000002.10:g.73570428A>G	NCBI36
NG_011690.1:g.109041A>G , LRG_741:g.109041A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7453A>G	ENSP00000507671.1:p.Met2485Val
ENST00000682801.1:c.7453A>G	ENSP00000507862.1:p.Met2485Val
ENST00000682859.1:c.7453A>G	ENSP00000508222.1:p.Met2485Val
ENST00000683791.1:c.845A>G
ENST00000684460.1:c.4905A>G
ENST00000684548.1:c.7453A>G	ENSP00000507421.1:p.Met2485Val
ENST00000684590.1:c.1900A>G	ENSP00000507376.1:p.Met634Val
ENST00000684656.1:c.4905A>G
ENST00000613296.6:c.7834A>G MANE Select	ENSP00000482968.1:p.Met2612Val
ENST00000651434.1:c.896-29982A>G
ENST00000423048.5:c.2665A>G	ENSP00000399833.1:p.Met889Val
ENST00000484298.5:c.7708A>G	ENSP00000478155.1:p.Met2570Val
ENST00000613296.4:c.7834A>G	ENSP00000482968.1:p.Met2612Val
ENST00000614410.4:c.7834A>G	ENSP00000479094.1:p.Met2612Val
ENST00000620466.4:n.1637A>G
NM_015120.4:c.7837A>G , LRG_741t1:c.7837A>G	NP_055935.4:p.Met2613Val
NM_001378454.1:c.7834A>G MANE Select	NP_001365383.1:p.Met2612Val