Canonical Allele Identifier: CA406395311

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181346G>C (hg19) ; chr19:g.45678088G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678088G>C , CM000681.2:g.45678088G>C	GRCh38
NC_000019.9:g.46181346G>C , CM000681.1:g.46181346G>C	GRCh37
NC_000019.8:g.50873186G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1014G>C MANE Select	ENSP00000467494.1:p.Arg338Ser
ENST00000652180.1:c.831G>C	ENSP00000498426.1:p.Arg277Ser
ENST00000263281.7:c.1014G>C	ENSP00000263281.3:p.Arg338Ser
ENST00000304207.12:c.906G>C	ENSP00000305321.8:p.Arg302Ser
ENST00000585889.1:c.*85G>C	ENSP00000467342.1:n.*85G>C
ENST00000590918.5:c.1014G>C	ENSP00000467494.1:p.Arg338Ser
ENST00000591224.1:n.470G>C
ENST00000593127.1:n.115G>C
NM_000164.2:c.1014G>C	NP_000155.1:p.Arg338Ser
NM_000164.3:c.1014G>C	NP_000155.1:p.Arg338Ser
NM_001308418.1:c.906G>C	NP_001295347.1:p.Arg302Ser
XM_011526709.1:c.1140G>C	XP_011525011.1:p.Arg380Ser
XM_011526710.1:c.1140G>C	XP_011525012.1:p.Arg380Ser
XM_011526711.1:c.1032G>C	XP_011525013.1:p.Arg344Ser
XM_011526712.1:c.906G>C	XP_011525014.1:p.Arg302Ser
XM_011526713.1:c.891G>C	XP_011525015.1:p.Arg297Ser
XM_011526714.1:c.723G>C	XP_011525016.1:p.Arg241Ser
XM_011526715.1:c.723G>C	XP_011525017.1:p.Arg241Ser
XR_935791.1:n.1033G>C
XM_011526709.2:c.1140G>C	XP_011525011.1:p.Arg380Ser
XM_011526710.2:c.1140G>C	XP_011525012.1:p.Arg380Ser
XM_011526711.2:c.1032G>C	XP_011525013.1:p.Arg344Ser
XM_011526713.2:c.891G>C	XP_011525015.1:p.Arg297Ser
XM_011526714.2:c.723G>C	XP_011525016.1:p.Arg241Ser
XM_011526715.2:c.723G>C	XP_011525017.1:p.Arg241Ser
XM_017026584.1:c.669G>C	XP_016882073.1:p.Arg223Ser
XM_017026585.1:c.648G>C	XP_016882074.1:p.Arg216Ser
XM_017026586.1:c.525G>C	XP_016882075.1:p.Arg175Ser
XM_017026587.1:c.522G>C	XP_016882076.1:p.Arg174Ser
XR_001753655.1:n.1109G>C
XR_935791.2:n.1039G>C
NM_000164.4:c.1014G>C MANE Select	NP_000155.1:p.Arg338Ser
NM_001308418.2:c.906G>C	NP_001295347.1:p.Arg302Ser