Canonical Allele Identifier: CA406395169

Gene: GIPR

Linked Data

• dbSNP Id: rs1183524419
• gnomAD v2: 19-46181224-C-T
• gnomAD v3: 19-45677966-C-T
• gnomAD v4: 19-45677966-C-T
• MyVariant Identifiers: chr19:g.46181224C>T (hg19) ; chr19:g.45677966C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677966C>T , CM000681.2:g.45677966C>T	GRCh38
NC_000019.9:g.46181224C>T , CM000681.1:g.46181224C>T	GRCh37
NC_000019.8:g.50873064C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.985C>T MANE Select	ENSP00000467494.1:p.Gln329Ter
ENST00000652180.1:c.802C>T	ENSP00000498426.1:p.Gln268Ter
ENST00000263281.7:c.985C>T	ENSP00000263281.3:p.Gln329Ter
ENST00000304207.12:c.877C>T	ENSP00000305321.8:p.Gln293Ter
ENST00000585889.1:c.*56C>T	ENSP00000467342.1:n.*56C>T
ENST00000590918.5:c.985C>T	ENSP00000467494.1:p.Gln329Ter
ENST00000591224.1:n.441C>T
ENST00000593127.1:n.86C>T
NM_000164.2:c.985C>T	NP_000155.1:p.Gln329Ter
NM_000164.3:c.985C>T	NP_000155.1:p.Gln329Ter
NM_001308418.1:c.877C>T	NP_001295347.1:p.Gln293Ter
XM_011526709.1:c.1111C>T	XP_011525011.1:p.Gln371Ter
XM_011526710.1:c.1111C>T	XP_011525012.1:p.Gln371Ter
XM_011526711.1:c.1003C>T	XP_011525013.1:p.Gln335Ter
XM_011526712.1:c.877C>T	XP_011525014.1:p.Gln293Ter
XM_011526713.1:c.862C>T	XP_011525015.1:p.Gln288Ter
XM_011526714.1:c.694C>T	XP_011525016.1:p.Gln232Ter
XM_011526715.1:c.694C>T	XP_011525017.1:p.Gln232Ter
XM_011526716.1:c.*69C>T	XP_011525018.1:n.*69C>T
XM_011526717.1:c.*69C>T	XP_011525019.1:n.*69C>T
XR_935791.1:n.1004C>T
XM_011526709.2:c.1111C>T	XP_011525011.1:p.Gln371Ter
XM_011526710.2:c.1111C>T	XP_011525012.1:p.Gln371Ter
XM_011526711.2:c.1003C>T	XP_011525013.1:p.Gln335Ter
XM_011526713.2:c.862C>T	XP_011525015.1:p.Gln288Ter
XM_011526714.2:c.694C>T	XP_011525016.1:p.Gln232Ter
XM_011526715.2:c.694C>T	XP_011525017.1:p.Gln232Ter
XM_011526716.2:c.*69C>T	XP_011525018.1:n.*69C>T
XM_017026584.1:c.640C>T	XP_016882073.1:p.Gln214Ter
XM_017026585.1:c.619C>T	XP_016882074.1:p.Gln207Ter
XM_017026586.1:c.496C>T	XP_016882075.1:p.Gln166Ter
XM_017026587.1:c.493C>T	XP_016882076.1:p.Gln165Ter
XR_001753655.1:n.1080C>T
XR_935791.2:n.1010C>T
NM_000164.4:c.985C>T MANE Select	NP_000155.1:p.Gln329Ter
NM_001308418.2:c.877C>T	NP_001295347.1:p.Gln293Ter