Canonical Allele Identifier: CA427000781

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73717174T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490047T>C , CM000664.2:g.73490047T>C	GRCh38
NC_000002.11:g.73717174T>C , CM000664.1:g.73717174T>C	GRCh37
NC_000002.10:g.73570682T>C	NCBI36
NG_011690.1:g.109295T>C , LRG_741:g.109295T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7707T>C	ENSP00000507671.1:p.Phe2569=
ENST00000682801.1:c.7707T>C	ENSP00000507862.1:p.Phe2569=
ENST00000682859.1:c.7707T>C	ENSP00000508222.1:p.Phe2569=
ENST00000683791.1:c.1099T>C
ENST00000684460.1:c.5159T>C
ENST00000684548.1:c.7707T>C	ENSP00000507421.1:p.Phe2569=
ENST00000684590.1:c.2154T>C	ENSP00000507376.1:p.Phe718=
ENST00000684656.1:c.5159T>C
ENST00000613296.6:c.8088T>C MANE Select	ENSP00000482968.1:p.Phe2696=
ENST00000651434.1:c.896-29728T>C
ENST00000423048.5:c.2919T>C	ENSP00000399833.1:p.Phe973=
ENST00000484298.5:c.7962T>C	ENSP00000478155.1:p.Phe2654=
ENST00000613296.4:c.8088T>C	ENSP00000482968.1:p.Phe2696=
ENST00000614410.4:c.8088T>C	ENSP00000479094.1:p.Phe2696=
ENST00000620466.4:n.1891T>C
NM_015120.4:c.8091T>C , LRG_741t1:c.8091T>C	NP_055935.4:p.Phe2697=
NM_001378454.1:c.8088T>C MANE Select	NP_001365383.1:p.Phe2696=