Canonical Allele Identifier: CA347267154

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73717137T>G (hg19) ; chr2:g.73490010T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490010T>G , CM000664.2:g.73490010T>G	GRCh38
NC_000002.11:g.73717137T>G , CM000664.1:g.73717137T>G	GRCh37
NC_000002.10:g.73570645T>G	NCBI36
NG_011690.1:g.109258T>G , LRG_741:g.109258T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7670T>G	ENSP00000507671.1:p.Val2557Gly
ENST00000682801.1:c.7670T>G	ENSP00000507862.1:p.Val2557Gly
ENST00000682859.1:c.7670T>G	ENSP00000508222.1:p.Val2557Gly
ENST00000683791.1:c.1062T>G
ENST00000684460.1:c.5122T>G
ENST00000684548.1:c.7670T>G	ENSP00000507421.1:p.Val2557Gly
ENST00000684590.1:c.2117T>G	ENSP00000507376.1:p.Val706Gly
ENST00000684656.1:c.5122T>G
ENST00000613296.6:c.8051T>G MANE Select	ENSP00000482968.1:p.Val2684Gly
ENST00000651434.1:c.896-29765T>G
ENST00000423048.5:c.2882T>G	ENSP00000399833.1:p.Val961Gly
ENST00000484298.5:c.7925T>G	ENSP00000478155.1:p.Val2642Gly
ENST00000613296.4:c.8051T>G	ENSP00000482968.1:p.Val2684Gly
ENST00000614410.4:c.8051T>G	ENSP00000479094.1:p.Val2684Gly
ENST00000620466.4:n.1854T>G
NM_015120.4:c.8054T>G , LRG_741t1:c.8054T>G	NP_055935.4:p.Val2685Gly
NM_001378454.1:c.8051T>G MANE Select	NP_001365383.1:p.Val2684Gly