Canonical Allele Identifier: CA1622517654
Community Standard Title: NM_002062.5(GLP1R):c.502G= (p.Gly168=)
Gene: GLP1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39066296G= , CM000668.2:g.39066296G= GRCh38
NC_000006.11:g.39034072G= , CM000668.1:g.39034072G= GRCh37
NC_000006.10:g.39142050G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002062.5:c.502G= MANE Select NP_002053.3:p.Gly168=
ENST00000373256.5:c.502G= MANE Select ENSP00000362353.4:p.Gly168=
NM_002062.3:c.502G= NP_002053.3:p.Gly168=
NM_002062.4:c.502G= NP_002053.3:p.Gly168=
NR_136562.1:n.562G=
NR_136562.2:n.562G=
NR_136563.1:n.562G=
NR_136563.2:n.562G=
ENST00000373256.4:c.502G= ENSP00000362353.4:p.Gly168=
XM_017010750.1:c.517G= XP_016866239.1:p.Gly173=
XM_017010751.1:c.517G= XP_016866240.1:p.Gly173=
XR_001743346.1:n.1097G=
XR_001743347.1:n.1097G=
XR_001743348.1:n.1097G=
XR_926153.1:n.562G=
XR_926154.1:n.562G=
XR_926155.1:n.562G=