Canonical Allele Identifier: CA347267233

Gene: ALMS1

Linked Data

• gnomAD v4: 2-73490022-T-C
• MyVariant Identifiers: chr2:g.73717149T>C (hg19) ; chr2:g.73490022T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490022T>C , CM000664.2:g.73490022T>C	GRCh38
NC_000002.11:g.73717149T>C , CM000664.1:g.73717149T>C	GRCh37
NC_000002.10:g.73570657T>C	NCBI36
NG_011690.1:g.109270T>C , LRG_741:g.109270T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7682T>C	ENSP00000507671.1:p.Phe2561Ser
ENST00000682801.1:c.7682T>C	ENSP00000507862.1:p.Phe2561Ser
ENST00000682859.1:c.7682T>C	ENSP00000508222.1:p.Phe2561Ser
ENST00000683791.1:c.1074T>C
ENST00000684460.1:c.5134T>C
ENST00000684548.1:c.7682T>C	ENSP00000507421.1:p.Phe2561Ser
ENST00000684590.1:c.2129T>C	ENSP00000507376.1:p.Phe710Ser
ENST00000684656.1:c.5134T>C
ENST00000613296.6:c.8063T>C MANE Select	ENSP00000482968.1:p.Phe2688Ser
ENST00000651434.1:c.896-29753T>C
ENST00000423048.5:c.2894T>C	ENSP00000399833.1:p.Phe965Ser
ENST00000484298.5:c.7937T>C	ENSP00000478155.1:p.Phe2646Ser
ENST00000613296.4:c.8063T>C	ENSP00000482968.1:p.Phe2688Ser
ENST00000614410.4:c.8063T>C	ENSP00000479094.1:p.Phe2688Ser
ENST00000620466.4:n.1866T>C
NM_015120.4:c.8066T>C , LRG_741t1:c.8066T>C	NP_055935.4:p.Phe2689Ser
NM_001378454.1:c.8063T>C MANE Select	NP_001365383.1:p.Phe2688Ser