Canonical Allele Identifier: CA426783622

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73828527A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73601400A>G , CM000664.2:g.73601400A>G	GRCh38
NC_000002.11:g.73828527A>G , CM000664.1:g.73828527A>G	GRCh37
NC_000002.10:g.73682035A>G	NCBI36
NG_011690.1:g.220648A>G , LRG_741:g.220648A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.11697A>G	ENSP00000507671.1:p.Arg3899=
ENST00000682801.1:c.11167-785A>G	ENSP00000507862.1:n.11167-785A>G
ENST00000682859.1:c.11697A>G	ENSP00000508222.1:p.Arg3899=
ENST00000683791.1:c.4783A>G
ENST00000684460.1:c.8978A>G
ENST00000684548.1:c.11697A>G	ENSP00000507421.1:p.Arg3899=
ENST00000684590.1:c.6144A>G	ENSP00000507376.1:p.Arg2048=
ENST00000684656.1:c.9162A>G
ENST00000613296.6:c.12078A>G MANE Select	ENSP00000482968.1:p.Arg4026=
ENST00000651057.1:c.2232A>G	ENSP00000498504.1:p.Arg744=
ENST00000651434.1:c.3434A>G
ENST00000651750.1:c.1260+519A>G
ENST00000652487.1:c.3249A>G
ENST00000464408.3:n.253A>G
ENST00000484298.5:c.11952A>G	ENSP00000478155.1:p.Arg3984=
ENST00000613296.4:c.12078A>G	ENSP00000482968.1:p.Arg4026=
ENST00000620466.4:n.5881A>G
NM_015120.4:c.12081A>G , LRG_741t1:c.12081A>G	NP_055935.4:p.Arg4027=
NM_001378454.1:c.12078A>G MANE Select	NP_001365383.1:p.Arg4026=