Canonical Allele Identifier: CA344236117
Gene: GPR37L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202128411G>T , CM000663.2:g.202128411G>T GRCh38
NC_000001.10:g.202097539G>T , CM000663.1:g.202097539G>T GRCh37
NC_000001.9:g.200364162G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682422.1:n.882G>T
ENST00000682545.1:c.*307G>T ENSP00000508402.1:n.*307G>T
ENST00000682887.1:c.1702G>T ENSP00000506946.1:n.1702G>T
ENST00000683302.1:c.1232G>T ENSP00000507885.1:p.Cys411Phe
ENST00000683557.1:c.*133G>T ENSP00000508029.1:n.*133G>T
ENST00000367282.6:c.1301G>T MANE Select ENSP00000356251.4:p.Cys434Phe
ENST00000367282.5:c.1301G>T ENSP00000356251.4:p.Cys434Phe
NM_004767.3:c.1301G>T NP_004758.3:p.Cys434Phe
XM_011510158.1:c.740G>T XP_011508460.1:p.Cys247Phe
NM_004767.4:c.1301G>T NP_004758.3:p.Cys434Phe
XM_011510158.2:c.740G>T XP_011508460.1:p.Cys247Phe
NM_004767.5:c.1301G>T MANE Select NP_004758.3:p.Cys434Phe