Canonical Allele Identifier: CA426783621

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73828525A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73601398A>C , CM000664.2:g.73601398A>C	GRCh38
NC_000002.11:g.73828525A>C , CM000664.1:g.73828525A>C	GRCh37
NC_000002.10:g.73682033A>C	NCBI36
NG_011690.1:g.220646A>C , LRG_741:g.220646A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.11695A>C	ENSP00000507671.1:p.Arg3899=
ENST00000682801.1:c.11167-787A>C	ENSP00000507862.1:n.11167-787A>C
ENST00000682859.1:c.11695A>C	ENSP00000508222.1:p.Arg3899=
ENST00000683791.1:c.4781A>C
ENST00000684460.1:c.8976A>C
ENST00000684548.1:c.11695A>C	ENSP00000507421.1:p.Arg3899=
ENST00000684590.1:c.6142A>C	ENSP00000507376.1:p.Arg2048=
ENST00000684656.1:c.9160A>C
ENST00000613296.6:c.12076A>C MANE Select	ENSP00000482968.1:p.Arg4026=
ENST00000651057.1:c.2230A>C	ENSP00000498504.1:p.Arg744=
ENST00000651434.1:c.3432A>C
ENST00000651750.1:c.1260+517A>C
ENST00000652487.1:c.3247A>C
ENST00000464408.3:n.251A>C
ENST00000484298.5:c.11950A>C	ENSP00000478155.1:p.Arg3984=
ENST00000613296.4:c.12076A>C	ENSP00000482968.1:p.Arg4026=
ENST00000620466.4:n.5879A>C
NM_015120.4:c.12079A>C , LRG_741t1:c.12079A>C	NP_055935.4:p.Arg4027=
NM_001378454.1:c.12076A>C MANE Select	NP_001365383.1:p.Arg4026=