Canonical Allele Identifier: CA2338547464

Gene: GIPR

Linked Data

• dbSNP Id: rs1975394604

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45668904_45668905insAG , CM000681.2:g.45668904_45668905insAG	GRCh38
NC_000019.9:g.46172162_46172163insAG , CM000681.1:g.46172162_46172163insAG	GRCh37
NC_000019.8:g.50864002_50864003insAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590918.6:c.-44-573_-44-572insAG MANE Select	ENSP00000467494.1:n.-44-573_-44-572insAG
ENST00000652180.1:c.-359-411_-359-410insAG	ENSP00000498426.1:n.-359-411_-359-410insAG
ENST00000263281.7:c.-44-573_-44-572insAG	ENSP00000263281.3:n.-44-573_-44-572insAG
ENST00000304207.12:c.-44-573_-44-572insAG	ENSP00000305321.8:n.-44-573_-44-572insAG
ENST00000585889.1:c.-44-573_-44-572insAG	ENSP00000467342.1:n.-44-573_-44-572insAG
ENST00000590918.5:c.-44-573_-44-572insAG	ENSP00000467494.1:n.-44-573_-44-572insAG
NM_000164.2:c.-44-573_-44-572insAG	NP_000155.1:n.-44-573_-44-572insAG
NM_000164.3:c.-44-573_-44-572insAG	NP_000155.1:n.-44-573_-44-572insAG
NM_001308418.1:c.-44-573_-44-572insAG	NP_001295347.1:n.-44-573_-44-572insAG
XM_011526709.1:c.-44-573_-44-572insAG	XP_011525011.1:n.-44-573_-44-572insAG
XM_011526710.1:c.-125-411_-125-410insAG	XP_011525012.1:n.-125-411_-125-410insAG
XM_011526711.1:c.-44-573_-44-572insAG	XP_011525013.1:n.-44-573_-44-572insAG
XM_011526712.1:c.-44-573_-44-572insAG	XP_011525014.1:n.-44-573_-44-572insAG
XM_011526713.1:c.-44-573_-44-572insAG	XP_011525015.1:n.-44-573_-44-572insAG
XM_011526714.1:c.-138+606_-138+607insAG	XP_011525016.1:n.-138+606_-138+607insAG
XM_011526715.1:c.-148+606_-148+607insAG	XP_011525017.1:n.-148+606_-148+607insAG
XM_011526716.1:c.-44-573_-44-572insAG	XP_011525018.1:n.-44-573_-44-572insAG
XM_011526717.1:c.-44-573_-44-572insAG	XP_011525019.1:n.-44-573_-44-572insAG
XR_935791.1:n.107-573_107-572insAG
XM_011526709.2:c.-44-573_-44-572insAG	XP_011525011.1:n.-44-573_-44-572insAG
XM_011526710.2:c.-125-411_-125-410insAG	XP_011525012.1:n.-125-411_-125-410insAG
XM_011526711.2:c.-44-573_-44-572insAG	XP_011525013.1:n.-44-573_-44-572insAG
XM_011526713.2:c.-44-573_-44-572insAG	XP_011525015.1:n.-44-573_-44-572insAG
XM_011526714.2:c.-138+606_-138+607insAG	XP_011525016.1:n.-138+606_-138+607insAG
XM_011526715.2:c.-148+606_-148+607insAG	XP_011525017.1:n.-148+606_-148+607insAG
XM_011526716.2:c.-44-573_-44-572insAG	XP_011525018.1:n.-44-573_-44-572insAG
XR_001753655.1:n.113-573_113-572insAG
XR_935791.2:n.113-573_113-572insAG
NM_000164.4:c.-44-573_-44-572insAG MANE Select	NP_000155.1:n.-44-573_-44-572insAG
NM_001308418.2:c.-44-573_-44-572insAG	NP_001295347.1:n.-44-573_-44-572insAG