Canonical Allele Identifier: CA413725023
Gene: CYSLTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78272822A>G , CM000685.2:g.78272822A>G GRCh38
NC_000023.10:g.77528319A>G , CM000685.1:g.77528319A>G GRCh37
NC_000023.9:g.77414975A>G NCBI36
NG_012809.1:g.59769T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373304.4:c.925T>C MANE Select ENSP00000362401.3:p.Phe309Leu
ENST00000373304.3:c.925T>C ENSP00000362401.3:p.Phe309Leu
ENST00000614798.1:c.925T>C ENSP00000478492.1:p.Phe309Leu
NM_001282186.1:c.925T>C NP_001269115.1:p.Phe309Leu
NM_001282187.1:c.925T>C NP_001269116.1:p.Phe309Leu
NM_001282188.1:c.925T>C NP_001269117.1:p.Phe309Leu
NM_006639.3:c.925T>C NP_006630.1:p.Phe309Leu
NM_006639.4:c.925T>C MANE Select NP_006630.1:p.Phe309Leu
NM_001282187.2:c.925T>C NP_001269116.1:p.Phe309Leu
NM_001282188.2:c.925T>C NP_001269117.1:p.Phe309Leu
NM_001282186.2:c.925T>C NP_001269115.1:p.Phe309Leu