Canonical Allele Identifier: CA2649858833
Gene: GPR37L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202128404_202128407dup , CM000663.2:g.202128404_202128407dup GRCh38
NC_000001.10:g.202097532_202097535dup , CM000663.1:g.202097532_202097535dup GRCh37
NC_000001.9:g.200364155_200364158dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682422.1:n.875_878dup
ENST00000682545.1:c.*300_*303dup ENSP00000508402.1:n.*300_*303dup
ENST00000682887.1:c.1695_1698dup ENSP00000506946.1:n.1695_1698dup
ENST00000683302.1:c.1225_1228dup ENSP00000507885.1:p.Cys410LeufsTer6
ENST00000683557.1:c.*126_*129dup ENSP00000508029.1:n.*126_*129dup
ENST00000367282.6:c.1294_1297dup MANE Select ENSP00000356251.4:p.Cys433LeufsTer6
ENST00000367282.5:c.1294_1297dup ENSP00000356251.4:p.Cys433LeufsTer6
NM_004767.3:c.1294_1297dup NP_004758.3:p.Cys433LeufsTer6
XM_011510158.1:c.733_736dup XP_011508460.1:p.Cys246LeufsTer6
NM_004767.4:c.1294_1297dup NP_004758.3:p.Cys433LeufsTer6
XM_011510158.2:c.733_736dup XP_011508460.1:p.Cys246LeufsTer6
NM_004767.5:c.1294_1297dup MANE Select NP_004758.3:p.Cys433LeufsTer6