Canonical Allele Identifier: CA1714023

Gene: ALMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73452710G>C , CM000664.2:g.73452710G>C	GRCh38
NC_000002.11:g.73679837G>C , CM000664.1:g.73679837G>C	GRCh37
NC_000002.10:g.73533345G>C	NCBI36
NG_011690.1:g.71958G>C , LRG_741:g.71958G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001378454.1:c.6183G>C MANE Select	NP_001365383.1:p.Gln2061His
ENST00000613296.6:c.6183G>C MANE Select	ENSP00000482968.1:p.Gln2061His
NM_015120.4:c.6186G>C , LRG_741t1:c.6186G>C	NP_055935.4:p.Gln2062His
ENST00000423048.5:c.1014G>C	ENSP00000399833.1:p.Gln338His
ENST00000484298.5:c.6057G>C	ENSP00000478155.1:p.Gln2019His
ENST00000613296.4:c.6183G>C	ENSP00000482968.1:p.Gln2061His
ENST00000614410.4:c.6183G>C	ENSP00000479094.1:p.Gln2061His
ENST00000682565.1:c.5802G>C	ENSP00000507671.1:p.Gln1934His
ENST00000682801.1:c.5802G>C	ENSP00000507862.1:p.Gln1934His
ENST00000682859.1:c.5802G>C	ENSP00000508222.1:p.Gln1934His
ENST00000683791.1:c.685+20419G>C
ENST00000684197.1:n.1152G>C
ENST00000684460.1:c.3254G>C
ENST00000684548.1:c.5802G>C	ENSP00000507421.1:p.Gln1934His
ENST00000684590.1:c.300G>C	ENSP00000507376.1:p.Gln100His
ENST00000684656.1:c.3254G>C