Canonical Allele Identifier: CA344235919
Gene: GPR37L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202128319C>A , CM000663.2:g.202128319C>A GRCh38
NC_000001.10:g.202097447C>A , CM000663.1:g.202097447C>A GRCh37
NC_000001.9:g.200364070C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682422.1:n.790C>A
ENST00000682545.1:c.*215C>A ENSP00000508402.1:n.*215C>A
ENST00000682887.1:c.1610C>A ENSP00000506946.1:n.1610C>A
ENST00000683302.1:c.1140C>A ENSP00000507885.1:p.Phe380Leu
ENST00000683557.1:c.*41C>A ENSP00000508029.1:n.*41C>A
ENST00000367282.6:c.1209C>A MANE Select ENSP00000356251.4:p.Phe403Leu
ENST00000367282.5:c.1209C>A ENSP00000356251.4:p.Phe403Leu
NM_004767.3:c.1209C>A NP_004758.3:p.Phe403Leu
XM_011510158.1:c.648C>A XP_011508460.1:p.Phe216Leu
NM_004767.4:c.1209C>A NP_004758.3:p.Phe403Leu
XM_011510158.2:c.648C>A XP_011508460.1:p.Phe216Leu
NM_004767.5:c.1209C>A MANE Select NP_004758.3:p.Phe403Leu