Canonical Allele Identifier: CA507825200

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181400G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678142G>C , CM000681.2:g.45678142G>C	GRCh38
NC_000019.9:g.46181400G>C , CM000681.1:g.46181400G>C	GRCh37
NC_000019.8:g.50873240G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1068G>C MANE Select	ENSP00000467494.1:p.Val356=
ENST00000652180.1:c.885G>C	ENSP00000498426.1:p.Val295=
ENST00000263281.7:c.1068G>C	ENSP00000263281.3:p.Val356=
ENST00000304207.12:c.960G>C	ENSP00000305321.8:p.Val320=
ENST00000585889.1:c.*139G>C	ENSP00000467342.1:n.*139G>C
ENST00000590918.5:c.1068G>C	ENSP00000467494.1:p.Val356=
ENST00000591224.1:n.524G>C
NM_000164.2:c.1068G>C	NP_000155.1:p.Val356=
NM_000164.3:c.1068G>C	NP_000155.1:p.Val356=
NM_001308418.1:c.960G>C	NP_001295347.1:p.Val320=
XM_011526709.1:c.1194G>C	XP_011525011.1:p.Val398=
XM_011526710.1:c.1194G>C	XP_011525012.1:p.Val398=
XM_011526711.1:c.1086G>C	XP_011525013.1:p.Val362=
XM_011526712.1:c.960G>C	XP_011525014.1:p.Val320=
XM_011526713.1:c.945G>C	XP_011525015.1:p.Val315=
XM_011526714.1:c.777G>C	XP_011525016.1:p.Val259=
XM_011526715.1:c.777G>C	XP_011525017.1:p.Val259=
XR_935791.1:n.1087G>C
XM_011526709.2:c.1194G>C	XP_011525011.1:p.Val398=
XM_011526710.2:c.1194G>C	XP_011525012.1:p.Val398=
XM_011526711.2:c.1086G>C	XP_011525013.1:p.Val362=
XM_011526713.2:c.945G>C	XP_011525015.1:p.Val315=
XM_011526714.2:c.777G>C	XP_011525016.1:p.Val259=
XM_011526715.2:c.777G>C	XP_011525017.1:p.Val259=
XM_017026584.1:c.723G>C	XP_016882073.1:p.Val241=
XM_017026585.1:c.702G>C	XP_016882074.1:p.Val234=
XM_017026586.1:c.579G>C	XP_016882075.1:p.Val193=
XM_017026587.1:c.576G>C	XP_016882076.1:p.Val192=
XR_001753655.1:n.1163G>C
XR_935791.2:n.1093G>C
NM_000164.4:c.1068G>C MANE Select	NP_000155.1:p.Val356=
NM_001308418.2:c.960G>C	NP_001295347.1:p.Val320=