Canonical Allele Identifier: CA344230732
Gene: GPR37L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202123328C>G , CM000663.2:g.202123328C>G GRCh38
NC_000001.10:g.202092456C>G , CM000663.1:g.202092456C>G GRCh37
NC_000001.9:g.200359079C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_004767.5:c.365C>G MANE Select NP_004758.3:p.Pro122Arg
ENST00000367282.6:c.365C>G MANE Select ENSP00000356251.4:p.Pro122Arg
NM_004767.3:c.365C>G NP_004758.3:p.Pro122Arg
NM_004767.4:c.365C>G NP_004758.3:p.Pro122Arg
ENST00000367282.5:c.365C>G ENSP00000356251.4:p.Pro122Arg
ENST00000682545.1:c.365C>G ENSP00000508402.1:p.Pro122Arg
ENST00000682887.1:c.365C>G ENSP00000506946.1:p.Pro122Arg
ENST00000683302.1:c.365C>G ENSP00000507885.1:p.Pro122Arg
ENST00000683557.1:c.365C>G ENSP00000508029.1:p.Pro122Arg
XM_011510158.1:c.70-4413C>G XP_011508460.1:n.70-4413C>G
XM_011510158.2:c.70-4413C>G XP_011508460.1:n.70-4413C>G