Canonical Allele Identifier: CA427000780

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73717171T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490044T>C , CM000664.2:g.73490044T>C	GRCh38
NC_000002.11:g.73717171T>C , CM000664.1:g.73717171T>C	GRCh37
NC_000002.10:g.73570679T>C	NCBI36
NG_011690.1:g.109292T>C , LRG_741:g.109292T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7704T>C	ENSP00000507671.1:p.Asp2568=
ENST00000682801.1:c.7704T>C	ENSP00000507862.1:p.Asp2568=
ENST00000682859.1:c.7704T>C	ENSP00000508222.1:p.Asp2568=
ENST00000683791.1:c.1096T>C
ENST00000684460.1:c.5156T>C
ENST00000684548.1:c.7704T>C	ENSP00000507421.1:p.Asp2568=
ENST00000684590.1:c.2151T>C	ENSP00000507376.1:p.Asp717=
ENST00000684656.1:c.5156T>C
ENST00000613296.6:c.8085T>C MANE Select	ENSP00000482968.1:p.Asp2695=
ENST00000651434.1:c.896-29731T>C
ENST00000423048.5:c.2916T>C	ENSP00000399833.1:p.Asp972=
ENST00000484298.5:c.7959T>C	ENSP00000478155.1:p.Asp2653=
ENST00000613296.4:c.8085T>C	ENSP00000482968.1:p.Asp2695=
ENST00000614410.4:c.8085T>C	ENSP00000479094.1:p.Asp2695=
ENST00000620466.4:n.1888T>C
NM_015120.4:c.8088T>C , LRG_741t1:c.8088T>C	NP_055935.4:p.Asp2696=
NM_001378454.1:c.8085T>C MANE Select	NP_001365383.1:p.Asp2695=