Canonical Allele Identifier: CA2719475536

Gene: GRHPR

Linked Data

• dbSNP Id: rs2118891328

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432138_37432139insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC , CM000671.2:g.37432138_37432139insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC	GRCh38
NC_000009.11:g.37432135_37432136insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC , CM000671.1:g.37432135_37432136insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC	GRCh37
NC_000009.10:g.37422135_37422136insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC	NCBI36
NG_008135.1:g.14429_14430insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.865_865+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC MANE Select	ENSP00000313432.6:n.865_865+1insTGATTCTGC...
ENST00000318158.10:c.865_865+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC	ENSP00000313432.6:n.865_865+1insTGATTCTGC...
ENST00000460882.5:n.892_892+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC
ENST00000480596.5:n.1566_1566+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC
ENST00000482603.1:n.318_318+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC
ENST00000491488.5:n.570_570+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC
ENST00000494290.1:c.*51+987_*51+988insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC	ENSP00000432021.1:n.*51+987_*51+988insTGA...
ENST00000497693.1:n.4433_4433+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC
ENST00000512404.2:n.52_53insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC
ENST00000607784.1:c.865_865+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC	ENSP00000475569.1:n.865_865+1insTGATTCTGC...
NM_012203.1:c.865_865+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC	NP_036335.1:n.865_865+1insTGATTCTGCCCCACA...
XM_005251631.1:c.544_544+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC	XP_005251688.1:n.544_544+1insTGATTCTGCCCC...
XM_011518073.1:c.463_463+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC	XP_011516375.1:n.463_463+1insTGATTCTGCCCC...
XM_017015320.2:c.865_865+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC	XP_016870809.1:n.865_865+1insTGATTCTGCCCC...
XM_017015321.2:c.865_865+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC	XP_016870810.1:n.865_865+1insTGATTCTGCCCC...
XM_017015323.2:c.463_463+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC	XP_016870812.1:n.463_463+1insTGATTCTGCCCC...
XM_024447716.1:c.1138_1138+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC	XP_024303484.1:n.1138_1138+1insTGATTCTGCC...
XM_024447717.1:c.1138_1138+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC	XP_024303485.1:n.1138_1138+1insTGATTCTGCC...
XR_002956828.1:n.1153_1153+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC
XR_002956829.1:n.1153_1153+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC
XR_002956830.1:n.2285_2285+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC
XR_002956831.1:n.1960_1960+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC
XR_002956832.1:n.1284_1284+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC
NM_012203.2:c.865_865+1insTGATTCTGCCCCACATTGGCAGTGCCACCCACAGAACCC MANE Select	NP_036335.1:n.865_865+1insTGATTCTGCCCCACA...