Canonical Allele Identifier: CA406395542

Gene: GIPR

Linked Data

• gnomAD v4: 19-45678152-G-T
• MyVariant Identifiers: chr19:g.46181410G>T (hg19) ; chr19:g.45678152G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678152G>T , CM000681.2:g.45678152G>T	GRCh38
NC_000019.9:g.46181410G>T , CM000681.1:g.46181410G>T	GRCh37
NC_000019.8:g.50873250G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1078G>T MANE Select	ENSP00000467494.1:p.Val360Leu
ENST00000652180.1:c.895G>T	ENSP00000498426.1:p.Val299Leu
ENST00000263281.7:c.1078G>T	ENSP00000263281.3:p.Val360Leu
ENST00000304207.12:c.970G>T	ENSP00000305321.8:p.Val324Leu
ENST00000585889.1:c.*149G>T	ENSP00000467342.1:n.*149G>T
ENST00000590918.5:c.1078G>T	ENSP00000467494.1:p.Val360Leu
ENST00000591224.1:n.534G>T
NM_000164.2:c.1078G>T	NP_000155.1:p.Val360Leu
NM_000164.3:c.1078G>T	NP_000155.1:p.Val360Leu
NM_001308418.1:c.970G>T	NP_001295347.1:p.Val324Leu
XM_011526709.1:c.1204G>T	XP_011525011.1:p.Val402Leu
XM_011526710.1:c.1204G>T	XP_011525012.1:p.Val402Leu
XM_011526711.1:c.1096G>T	XP_011525013.1:p.Val366Leu
XM_011526712.1:c.970G>T	XP_011525014.1:p.Val324Leu
XM_011526713.1:c.955G>T	XP_011525015.1:p.Val319Leu
XM_011526714.1:c.787G>T	XP_011525016.1:p.Val263Leu
XM_011526715.1:c.787G>T	XP_011525017.1:p.Val263Leu
XR_935791.1:n.1097G>T
XM_011526709.2:c.1204G>T	XP_011525011.1:p.Val402Leu
XM_011526710.2:c.1204G>T	XP_011525012.1:p.Val402Leu
XM_011526711.2:c.1096G>T	XP_011525013.1:p.Val366Leu
XM_011526713.2:c.955G>T	XP_011525015.1:p.Val319Leu
XM_011526714.2:c.787G>T	XP_011525016.1:p.Val263Leu
XM_011526715.2:c.787G>T	XP_011525017.1:p.Val263Leu
XM_017026584.1:c.733G>T	XP_016882073.1:p.Val245Leu
XM_017026585.1:c.712G>T	XP_016882074.1:p.Val238Leu
XM_017026586.1:c.589G>T	XP_016882075.1:p.Val197Leu
XM_017026587.1:c.586G>T	XP_016882076.1:p.Val196Leu
XR_001753655.1:n.1173G>T
XR_935791.2:n.1103G>T
NM_000164.4:c.1078G>T MANE Select	NP_000155.1:p.Val360Leu
NM_001308418.2:c.970G>T	NP_001295347.1:p.Val324Leu