Canonical Allele Identifier: CA406395194

Gene: GIPR

Linked Data

• gnomAD v4: 19-45677971-G-T
• MyVariant Identifiers: chr19:g.46181229G>T (hg19) ; chr19:g.45677971G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677971G>T , CM000681.2:g.45677971G>T	GRCh38
NC_000019.9:g.46181229G>T , CM000681.1:g.46181229G>T	GRCh37
NC_000019.8:g.50873069G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.990G>T MANE Select	ENSP00000467494.1:p.Met330Ile
ENST00000652180.1:c.807G>T	ENSP00000498426.1:p.Met269Ile
ENST00000263281.7:c.990G>T	ENSP00000263281.3:p.Met330Ile
ENST00000304207.12:c.882G>T	ENSP00000305321.8:p.Met294Ile
ENST00000585889.1:c.*61G>T	ENSP00000467342.1:n.*61G>T
ENST00000590918.5:c.990G>T	ENSP00000467494.1:p.Met330Ile
ENST00000591224.1:n.446G>T
ENST00000593127.1:n.91G>T
NM_000164.2:c.990G>T	NP_000155.1:p.Met330Ile
NM_000164.3:c.990G>T	NP_000155.1:p.Met330Ile
NM_001308418.1:c.882G>T	NP_001295347.1:p.Met294Ile
XM_011526709.1:c.1116G>T	XP_011525011.1:p.Met372Ile
XM_011526710.1:c.1116G>T	XP_011525012.1:p.Met372Ile
XM_011526711.1:c.1008G>T	XP_011525013.1:p.Met336Ile
XM_011526712.1:c.882G>T	XP_011525014.1:p.Met294Ile
XM_011526713.1:c.867G>T	XP_011525015.1:p.Met289Ile
XM_011526714.1:c.699G>T	XP_011525016.1:p.Met233Ile
XM_011526715.1:c.699G>T	XP_011525017.1:p.Met233Ile
XM_011526716.1:c.*74G>T	XP_011525018.1:n.*74G>T
XM_011526717.1:c.*74G>T	XP_011525019.1:n.*74G>T
XR_935791.1:n.1009G>T
XM_011526709.2:c.1116G>T	XP_011525011.1:p.Met372Ile
XM_011526710.2:c.1116G>T	XP_011525012.1:p.Met372Ile
XM_011526711.2:c.1008G>T	XP_011525013.1:p.Met336Ile
XM_011526713.2:c.867G>T	XP_011525015.1:p.Met289Ile
XM_011526714.2:c.699G>T	XP_011525016.1:p.Met233Ile
XM_011526715.2:c.699G>T	XP_011525017.1:p.Met233Ile
XM_011526716.2:c.*74G>T	XP_011525018.1:n.*74G>T
XM_017026584.1:c.645G>T	XP_016882073.1:p.Met215Ile
XM_017026585.1:c.624G>T	XP_016882074.1:p.Met208Ile
XM_017026586.1:c.501G>T	XP_016882075.1:p.Met167Ile
XM_017026587.1:c.498G>T	XP_016882076.1:p.Met166Ile
XR_001753655.1:n.1085G>T
XR_935791.2:n.1015G>T
NM_000164.4:c.990G>T MANE Select	NP_000155.1:p.Met330Ile
NM_001308418.2:c.882G>T	NP_001295347.1:p.Met294Ile