Canonical Allele Identifier: CA344235973
Gene: GPR37L1 HGNC NCBI

Linked Data

dbSNP Id: rs1228691400

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202128344A>C , CM000663.2:g.202128344A>C GRCh38
NC_000001.10:g.202097472A>C , CM000663.1:g.202097472A>C GRCh37
NC_000001.9:g.200364095A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682422.1:n.815A>C
ENST00000682545.1:c.*240A>C ENSP00000508402.1:n.*240A>C
ENST00000682887.1:c.1635A>C ENSP00000506946.1:n.1635A>C
ENST00000683302.1:c.1165A>C ENSP00000507885.1:p.Thr389Pro
ENST00000683557.1:c.*66A>C ENSP00000508029.1:n.*66A>C
ENST00000367282.6:c.1234A>C MANE Select ENSP00000356251.4:p.Thr412Pro
ENST00000367282.5:c.1234A>C ENSP00000356251.4:p.Thr412Pro
NM_004767.3:c.1234A>C NP_004758.3:p.Thr412Pro
XM_011510158.1:c.673A>C XP_011508460.1:p.Thr225Pro
NM_004767.4:c.1234A>C NP_004758.3:p.Thr412Pro
XM_011510158.2:c.673A>C XP_011508460.1:p.Thr225Pro
NM_004767.5:c.1234A>C MANE Select NP_004758.3:p.Thr412Pro