Canonical Allele Identifier: CA347282952

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73799458A>C (hg19) ; chr2:g.73572331A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73572331A>C , CM000664.2:g.73572331A>C	GRCh38
NC_000002.11:g.73799458A>C , CM000664.1:g.73799458A>C	GRCh37
NC_000002.10:g.73652966A>C	NCBI36
NG_011690.1:g.191579A>C , LRG_741:g.191579A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.10073A>C	ENSP00000507671.1:p.His3358Pro
ENST00000682801.1:c.10073A>C	ENSP00000507862.1:p.His3358Pro
ENST00000682859.1:c.10073A>C	ENSP00000508222.1:p.His3358Pro
ENST00000683791.1:c.3159A>C
ENST00000684460.1:c.7354A>C
ENST00000684548.1:c.10073A>C	ENSP00000507421.1:p.His3358Pro
ENST00000684590.1:c.4520A>C	ENSP00000507376.1:p.His1507Pro
ENST00000684656.1:c.7399A>C
ENST00000613296.6:c.10454A>C MANE Select	ENSP00000482968.1:p.His3485Pro
ENST00000651057.1:c.608A>C	ENSP00000498504.1:p.His203Pro
ENST00000651434.1:c.1810A>C
ENST00000652487.1:c.1551A>C
ENST00000423048.5:c.3945A>C	ENSP00000399833.1:n.3945A>C
ENST00000484298.5:c.10328A>C	ENSP00000478155.1:p.His3443Pro
ENST00000613296.4:c.10454A>C	ENSP00000482968.1:p.His3485Pro
ENST00000614410.4:c.10454A>C	ENSP00000479094.1:p.His3485Pro
ENST00000620466.4:n.4257A>C
NM_015120.4:c.10457A>C , LRG_741t1:c.10457A>C	NP_055935.4:p.His3486Pro
NM_001378454.1:c.10454A>C MANE Select	NP_001365383.1:p.His3485Pro