Canonical Allele Identifier: CA406395321

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181348T>G (hg19) ; chr19:g.45678090T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678090T>G , CM000681.2:g.45678090T>G	GRCh38
NC_000019.9:g.46181348T>G , CM000681.1:g.46181348T>G	GRCh37
NC_000019.8:g.50873188T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1016T>G MANE Select	ENSP00000467494.1:p.Leu339Arg
ENST00000652180.1:c.833T>G	ENSP00000498426.1:p.Leu278Arg
ENST00000263281.7:c.1016T>G	ENSP00000263281.3:p.Leu339Arg
ENST00000304207.12:c.908T>G	ENSP00000305321.8:p.Leu303Arg
ENST00000585889.1:c.*87T>G	ENSP00000467342.1:n.*87T>G
ENST00000590918.5:c.1016T>G	ENSP00000467494.1:p.Leu339Arg
ENST00000591224.1:n.472T>G
ENST00000593127.1:n.117T>G
NM_000164.2:c.1016T>G	NP_000155.1:p.Leu339Arg
NM_000164.3:c.1016T>G	NP_000155.1:p.Leu339Arg
NM_001308418.1:c.908T>G	NP_001295347.1:p.Leu303Arg
XM_011526709.1:c.1142T>G	XP_011525011.1:p.Leu381Arg
XM_011526710.1:c.1142T>G	XP_011525012.1:p.Leu381Arg
XM_011526711.1:c.1034T>G	XP_011525013.1:p.Leu345Arg
XM_011526712.1:c.908T>G	XP_011525014.1:p.Leu303Arg
XM_011526713.1:c.893T>G	XP_011525015.1:p.Leu298Arg
XM_011526714.1:c.725T>G	XP_011525016.1:p.Leu242Arg
XM_011526715.1:c.725T>G	XP_011525017.1:p.Leu242Arg
XR_935791.1:n.1035T>G
XM_011526709.2:c.1142T>G	XP_011525011.1:p.Leu381Arg
XM_011526710.2:c.1142T>G	XP_011525012.1:p.Leu381Arg
XM_011526711.2:c.1034T>G	XP_011525013.1:p.Leu345Arg
XM_011526713.2:c.893T>G	XP_011525015.1:p.Leu298Arg
XM_011526714.2:c.725T>G	XP_011525016.1:p.Leu242Arg
XM_011526715.2:c.725T>G	XP_011525017.1:p.Leu242Arg
XM_017026584.1:c.671T>G	XP_016882073.1:p.Leu224Arg
XM_017026585.1:c.650T>G	XP_016882074.1:p.Leu217Arg
XM_017026586.1:c.527T>G	XP_016882075.1:p.Leu176Arg
XM_017026587.1:c.524T>G	XP_016882076.1:p.Leu175Arg
XR_001753655.1:n.1111T>G
XR_935791.2:n.1041T>G
NM_000164.4:c.1016T>G MANE Select	NP_000155.1:p.Leu339Arg
NM_001308418.2:c.908T>G	NP_001295347.1:p.Leu303Arg