Canonical Allele Identifier: CA2512361844
Gene: GPR37L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202128248_202128250del , CM000663.2:g.202128248_202128250del GRCh38
NC_000001.10:g.202097376_202097378del , CM000663.1:g.202097376_202097378del GRCh37
NC_000001.9:g.200363999_200364001del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682422.1:n.719_721del
ENST00000682545.1:c.*144_*146del ENSP00000508402.1:n.*144_*146del
ENST00000682887.1:c.1539_1541del ENSP00000506946.1:n.1539_1541del
ENST00000683302.1:c.1069_1071del ENSP00000507885.1:p.Ile357del
ENST00000683557.1:c.729_731del ENSP00000508029.1:p.Ser244del
ENST00000367282.6:c.1138_1140del MANE Select ENSP00000356251.4:p.Ile380del
ENST00000367282.5:c.1138_1140del ENSP00000356251.4:p.Ile380del
NM_004767.3:c.1138_1140del NP_004758.3:p.Ile380del
XM_011510158.1:c.577_579del XP_011508460.1:p.Ile193del
NM_004767.4:c.1138_1140del NP_004758.3:p.Ile380del
XM_011510158.2:c.577_579del XP_011508460.1:p.Ile193del
NM_004767.5:c.1138_1140del MANE Select NP_004758.3:p.Ile380del