Canonical Allele Identifier: CA2649858831
Gene: GPR37L1 HGNC NCBI

Linked Data

gnomAD v4: 1-202128344-A-AC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202128348dup , CM000663.2:g.202128348dup GRCh38
NC_000001.10:g.202097476dup , CM000663.1:g.202097476dup GRCh37
NC_000001.9:g.200364099dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682422.1:n.819dup
ENST00000682545.1:c.*244dup ENSP00000508402.1:n.*244dup
ENST00000682887.1:c.1639dup ENSP00000506946.1:n.1639dup
ENST00000683302.1:c.1169dup ENSP00000507885.1:p.Val391SerfsTer24
ENST00000683557.1:c.*70dup ENSP00000508029.1:n.*70dup
ENST00000367282.6:c.1238dup MANE Select ENSP00000356251.4:p.Val414SerfsTer24
ENST00000367282.5:c.1238dup ENSP00000356251.4:p.Val414SerfsTer24
NM_004767.3:c.1238dup NP_004758.3:p.Val414SerfsTer24
XM_011510158.1:c.677dup XP_011508460.1:p.Val227SerfsTer24
NM_004767.4:c.1238dup NP_004758.3:p.Val414SerfsTer24
XM_011510158.2:c.677dup XP_011508460.1:p.Val227SerfsTer24
NM_004767.5:c.1238dup MANE Select NP_004758.3:p.Val414SerfsTer24
Search 100 bp 5'
Search 100 bp 3'