Canonical Allele Identifier: CA1846884787

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436411_37436455delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC , CM000671.2:g.37436411_37436455delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC	GRCh38
NC_000009.11:g.37436408_37436452delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC , CM000671.1:g.37436408_37436452delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC	GRCh37
NC_000009.10:g.37426408_37426452delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC	NCBI36
NG_008135.1:g.18702_18746delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-250_866-206delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC MANE Select	ENSP00000313432.6:n.866-250_866-206delinsTAGAATACAAATCTTTCATC...
ENST00000318158.10:c.866-250_866-206delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC	ENSP00000313432.6:n.866-250_866-206delinsTAGAATACAAATCTTTCATC...
ENST00000460882.5:n.893-250_893-206delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC
ENST00000480596.5:n.1567-250_1567-206delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC
ENST00000491488.5:n.571-250_571-206delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC
ENST00000494290.1:c.*52-470_*52-426delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC	ENSP00000432021.1:n.*52-470_*52-426delinsTAGAATACAAATCTTTCATC...
ENST00000497693.1:n.4434-250_4434-206delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC
NM_012203.1:c.866-250_866-206delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC	NP_036335.1:n.866-250_866-206delinsTAGAATACAAATCTTTCATCACATTG...
XM_005251631.1:c.545-250_545-206delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC	XP_005251688.1:n.545-250_545-206delinsTAGAATACAAATCTTTCATCACA...
XM_011518073.1:c.464-250_464-206delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC	XP_011516375.1:n.464-250_464-206delinsTAGAATACAAATCTTTCATCACA...
XM_017015320.2:c.946-1000_946-956delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC	XP_016870809.1:n.946-1000_946-956delinsTAGAATACAAATCTTTCATCAC...
XM_017015321.2:c.866-1000_866-956delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC	XP_016870810.1:n.866-1000_866-956delinsTAGAATACAAATCTTTCATCAC...
XM_017015323.2:c.544-1000_544-956delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC	XP_016870812.1:n.544-1000_544-956delinsTAGAATACAAATCTTTCATCAC...
XM_024447716.1:c.1219-1000_1219-956delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC	XP_024303484.1:n.1219-1000_1219-956delinsTAGAATACAAATCTTTCATC...
XM_024447717.1:c.1139-1000_1139-956delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC	XP_024303485.1:n.1139-1000_1139-956delinsTAGAATACAAATCTTTCATC...
XR_002956828.1:n.1234-1000_1234-956delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC
XR_002956829.1:n.1154-1000_1154-956delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC
XR_002956830.1:n.2286-250_2286-206delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC
XR_002956831.1:n.1961-250_1961-206delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC
XR_002956832.1:n.1285-250_1285-206delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC
NM_012203.2:c.866-250_866-206delinsTAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC MANE Select	NP_036335.1:n.866-250_866-206delinsTAGAATACAAATCTTTCATCACATTG...