Canonical Allele Identifier: CA344235871
Gene: GPR37L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202128297T>A , CM000663.2:g.202128297T>A GRCh38
NC_000001.10:g.202097425T>A , CM000663.1:g.202097425T>A GRCh37
NC_000001.9:g.200364048T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682422.1:n.768T>A
ENST00000682545.1:c.*193T>A ENSP00000508402.1:n.*193T>A
ENST00000682887.1:c.1588T>A ENSP00000506946.1:n.1588T>A
ENST00000683302.1:c.1118T>A ENSP00000507885.1:p.Leu373His
ENST00000683557.1:c.*19T>A ENSP00000508029.1:n.*19T>A
ENST00000367282.6:c.1187T>A MANE Select ENSP00000356251.4:p.Leu396His
ENST00000367282.5:c.1187T>A ENSP00000356251.4:p.Leu396His
NM_004767.3:c.1187T>A NP_004758.3:p.Leu396His
XM_011510158.1:c.626T>A XP_011508460.1:p.Leu209His
NM_004767.4:c.1187T>A NP_004758.3:p.Leu396His
XM_011510158.2:c.626T>A XP_011508460.1:p.Leu209His
NM_004767.5:c.1187T>A MANE Select NP_004758.3:p.Leu396His