Canonical Allele Identifier: CA427024704

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799571A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572444A>C , CM000664.2:g.73572444A>C	GRCh38
NC_000002.11:g.73799571A>C , CM000664.1:g.73799571A>C	GRCh37
NC_000002.10:g.73653079A>C	NCBI36
NG_011690.1:g.191692A>C , LRG_741:g.191692A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10186A>C	ENSP00000507671.1:p.Arg3396=
ENST00000682801.1:c.10186A>C	ENSP00000507862.1:p.Arg3396=
ENST00000682859.1:c.10186A>C	ENSP00000508222.1:p.Arg3396=
ENST00000683791.1:c.3272A>C
ENST00000684460.1:c.7467A>C
ENST00000684548.1:c.10186A>C	ENSP00000507421.1:p.Arg3396=
ENST00000684590.1:c.4633A>C	ENSP00000507376.1:p.Arg1545=
ENST00000684656.1:c.7512A>C
ENST00000613296.6:c.10567A>C MANE Select	ENSP00000482968.1:p.Arg3523=
ENST00000651057.1:c.721A>C	ENSP00000498504.1:p.Arg241=
ENST00000651434.1:c.1923A>C
ENST00000652487.1:c.1664A>C
ENST00000423048.5:c.4058A>C	ENSP00000399833.1:n.4058A>C
ENST00000484298.5:c.10441A>C	ENSP00000478155.1:p.Arg3481=
ENST00000613296.4:c.10567A>C	ENSP00000482968.1:p.Arg3523=
ENST00000614410.4:c.10567A>C	ENSP00000479094.1:p.Arg3523=
ENST00000620466.4:n.4370A>C
NM_015120.4:c.10570A>C , LRG_741t1:c.10570A>C	NP_055935.4:p.Arg3524=
NM_001378454.1:c.10567A>C MANE Select	NP_001365383.1:p.Arg3523=