Canonical Allele Identifier: CA344236100
Gene: GPR37L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202128405G>A , CM000663.2:g.202128405G>A GRCh38
NC_000001.10:g.202097533G>A , CM000663.1:g.202097533G>A GRCh37
NC_000001.9:g.200364156G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682422.1:n.876G>A
ENST00000682545.1:c.*301G>A ENSP00000508402.1:n.*301G>A
ENST00000682887.1:c.1696G>A ENSP00000506946.1:n.1696G>A
ENST00000683302.1:c.1226G>A ENSP00000507885.1:p.Cys409Tyr
ENST00000683557.1:c.*127G>A ENSP00000508029.1:n.*127G>A
ENST00000367282.6:c.1295G>A MANE Select ENSP00000356251.4:p.Cys432Tyr
ENST00000367282.5:c.1295G>A ENSP00000356251.4:p.Cys432Tyr
NM_004767.3:c.1295G>A NP_004758.3:p.Cys432Tyr
XM_011510158.1:c.734G>A XP_011508460.1:p.Cys245Tyr
NM_004767.4:c.1295G>A NP_004758.3:p.Cys432Tyr
XM_011510158.2:c.734G>A XP_011508460.1:p.Cys245Tyr
NM_004767.5:c.1295G>A MANE Select NP_004758.3:p.Cys432Tyr