Canonical Allele Identifier: CA406395125
Gene: GIPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45677952A>T , CM000681.2:g.45677952A>T GRCh38
NC_000019.9:g.46181210A>T , CM000681.1:g.46181210A>T GRCh37
NC_000019.8:g.50873050A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000590918.6:c.971A>T MANE Select ENSP00000467494.1:p.Lys324Met
ENST00000652180.1:c.788A>T ENSP00000498426.1:p.Lys263Met
ENST00000263281.7:c.971A>T ENSP00000263281.3:p.Lys324Met
ENST00000304207.12:c.863A>T ENSP00000305321.8:p.Lys288Met
ENST00000585889.1:c.*42A>T ENSP00000467342.1:n.*42A>T
ENST00000590918.5:c.971A>T ENSP00000467494.1:p.Lys324Met
ENST00000591224.1:n.427A>T
ENST00000593127.1:n.72A>T
NM_000164.2:c.971A>T NP_000155.1:p.Lys324Met
NM_000164.3:c.971A>T NP_000155.1:p.Lys324Met
NM_001308418.1:c.863A>T NP_001295347.1:p.Lys288Met
XM_011526709.1:c.1097A>T XP_011525011.1:p.Lys366Met
XM_011526710.1:c.1097A>T XP_011525012.1:p.Lys366Met
XM_011526711.1:c.989A>T XP_011525013.1:p.Lys330Met
XM_011526712.1:c.863A>T XP_011525014.1:p.Lys288Met
XM_011526713.1:c.848A>T XP_011525015.1:p.Lys283Met
XM_011526714.1:c.680A>T XP_011525016.1:p.Lys227Met
XM_011526715.1:c.680A>T XP_011525017.1:p.Lys227Met
XM_011526716.1:c.*55A>T XP_011525018.1:n.*55A>T
XM_011526717.1:c.*55A>T XP_011525019.1:n.*55A>T
XR_935791.1:n.990A>T
XM_011526709.2:c.1097A>T XP_011525011.1:p.Lys366Met
XM_011526710.2:c.1097A>T XP_011525012.1:p.Lys366Met
XM_011526711.2:c.989A>T XP_011525013.1:p.Lys330Met
XM_011526713.2:c.848A>T XP_011525015.1:p.Lys283Met
XM_011526714.2:c.680A>T XP_011525016.1:p.Lys227Met
XM_011526715.2:c.680A>T XP_011525017.1:p.Lys227Met
XM_011526716.2:c.*55A>T XP_011525018.1:n.*55A>T
XM_017026584.1:c.626A>T XP_016882073.1:p.Lys209Met
XM_017026585.1:c.605A>T XP_016882074.1:p.Lys202Met
XM_017026586.1:c.482A>T XP_016882075.1:p.Lys161Met
XM_017026587.1:c.479A>T XP_016882076.1:p.Lys160Met
XR_001753655.1:n.1066A>T
XR_935791.2:n.996A>T
NM_000164.4:c.971A>T MANE Select NP_000155.1:p.Lys324Met
NM_001308418.2:c.863A>T NP_001295347.1:p.Lys288Met