Canonical Allele Identifier: CA344236010
Gene: GPR37L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202128365A>C , CM000663.2:g.202128365A>C GRCh38
NC_000001.10:g.202097493A>C , CM000663.1:g.202097493A>C GRCh37
NC_000001.9:g.200364116A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682422.1:n.836A>C
ENST00000682545.1:c.*261A>C ENSP00000508402.1:n.*261A>C
ENST00000682887.1:c.1656A>C ENSP00000506946.1:n.1656A>C
ENST00000683302.1:c.1186A>C ENSP00000507885.1:p.Ile396Leu
ENST00000683557.1:c.*87A>C ENSP00000508029.1:n.*87A>C
ENST00000367282.6:c.1255A>C MANE Select ENSP00000356251.4:p.Ile419Leu
ENST00000367282.5:c.1255A>C ENSP00000356251.4:p.Ile419Leu
NM_004767.3:c.1255A>C NP_004758.3:p.Ile419Leu
XM_011510158.1:c.694A>C XP_011508460.1:p.Ile232Leu
NM_004767.4:c.1255A>C NP_004758.3:p.Ile419Leu
XM_011510158.2:c.694A>C XP_011508460.1:p.Ile232Leu
NM_004767.5:c.1255A>C MANE Select NP_004758.3:p.Ile419Leu