Canonical Allele Identifier: CA427024355

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799999T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572872T>A , CM000664.2:g.73572872T>A	GRCh38
NC_000002.11:g.73799999T>A , CM000664.1:g.73799999T>A	GRCh37
NC_000002.10:g.73653507T>A	NCBI36
NG_011690.1:g.192120T>A , LRG_741:g.192120T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10614T>A	ENSP00000507671.1:p.Gly3538=
ENST00000682801.1:c.10614T>A	ENSP00000507862.1:p.Gly3538=
ENST00000682859.1:c.10614T>A	ENSP00000508222.1:p.Gly3538=
ENST00000683791.1:c.3700T>A
ENST00000684460.1:c.7895T>A
ENST00000684548.1:c.10614T>A	ENSP00000507421.1:p.Gly3538=
ENST00000684590.1:c.5061T>A	ENSP00000507376.1:p.Gly1687=
ENST00000684656.1:c.7940T>A
ENST00000613296.6:c.10995T>A MANE Select	ENSP00000482968.1:p.Gly3665=
ENST00000651057.1:c.1149T>A	ENSP00000498504.1:p.Gly383=
ENST00000651434.1:c.2351T>A
ENST00000651750.1:c.383T>A
ENST00000652487.1:c.2092T>A
ENST00000423048.5:c.4486T>A	ENSP00000399833.1:n.4486T>A
ENST00000484298.5:c.10869T>A	ENSP00000478155.1:p.Gly3623=
ENST00000613296.4:c.10995T>A	ENSP00000482968.1:p.Gly3665=
ENST00000614410.4:c.10995T>A	ENSP00000479094.1:p.Gly3665=
ENST00000620466.4:n.4798T>A
NM_015120.4:c.10998T>A , LRG_741t1:c.10998T>A	NP_055935.4:p.Gly3666=
NM_001378454.1:c.10995T>A MANE Select	NP_001365383.1:p.Gly3665=