Canonical Allele Identifier: CA2649858834
Gene: GPR37L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202128422_202128424del , CM000663.2:g.202128422_202128424del GRCh38
NC_000001.10:g.202097550_202097552del , CM000663.1:g.202097550_202097552del GRCh37
NC_000001.9:g.200364173_200364175del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682422.1:n.893_895del
ENST00000682545.1:c.*318_*320del ENSP00000508402.1:n.*318_*320del
ENST00000682887.1:c.1713_1715del ENSP00000506946.1:n.1713_1715del
ENST00000683302.1:c.1243_1245del ENSP00000507885.1:p.Glu415del
ENST00000683557.1:c.*144_*146del ENSP00000508029.1:n.*144_*146del
ENST00000367282.6:c.1312_1314del MANE Select ENSP00000356251.4:p.Glu438del
ENST00000367282.5:c.1312_1314del ENSP00000356251.4:p.Glu438del
NM_004767.3:c.1312_1314del NP_004758.3:p.Glu438del
XM_011510158.1:c.751_753del XP_011508460.1:p.Glu251del
NM_004767.4:c.1312_1314del NP_004758.3:p.Glu438del
XM_011510158.2:c.751_753del XP_011508460.1:p.Glu251del
NM_004767.5:c.1312_1314del MANE Select NP_004758.3:p.Glu438del