Canonical Allele Identifier: CA1123330203

Gene: GRHPR

Linked Data

• dbSNP Id: rs1823671864
• gnomAD v3: 9-37436652-C-CT
• gnomAD v4: 9-37436652-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436652_37436653insT , CM000671.2:g.37436652_37436653insT	GRCh38
NC_000009.11:g.37436649_37436650insT , CM000671.1:g.37436649_37436650insT	GRCh37
NC_000009.10:g.37426649_37426650insT	NCBI36
NG_008135.1:g.18943_18944insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-9_866-8insT MANE Select	ENSP00000313432.6:n.866-9_866-8insT
ENST00000318158.10:c.866-9_866-8insT	ENSP00000313432.6:n.866-9_866-8insT
ENST00000460882.5:n.893-9_893-8insT
ENST00000480596.5:n.1567-9_1567-8insT
ENST00000491488.5:n.571-9_571-8insT
ENST00000494290.1:c.*52-229_*52-228insT	ENSP00000432021.1:n.*52-229_*52-228insT
ENST00000497693.1:n.4434-9_4434-8insT
NM_012203.1:c.866-9_866-8insT	NP_036335.1:n.866-9_866-8insT
XM_005251631.1:c.545-9_545-8insT	XP_005251688.1:n.545-9_545-8insT
XM_011518073.1:c.464-9_464-8insT	XP_011516375.1:n.464-9_464-8insT
XM_017015320.2:c.946-759_946-758insT	XP_016870809.1:n.946-759_946-758insT
XM_017015321.2:c.866-759_866-758insT	XP_016870810.1:n.866-759_866-758insT
XM_017015323.2:c.544-759_544-758insT	XP_016870812.1:n.544-759_544-758insT
XM_024447716.1:c.1219-759_1219-758insT	XP_024303484.1:n.1219-759_1219-758insT
XM_024447717.1:c.1139-759_1139-758insT	XP_024303485.1:n.1139-759_1139-758insT
XR_002956828.1:n.1234-759_1234-758insT
XR_002956829.1:n.1154-759_1154-758insT
XR_002956830.1:n.2286-9_2286-8insT
XR_002956831.1:n.1961-9_1961-8insT
XR_002956832.1:n.1285-9_1285-8insT
NM_012203.2:c.866-9_866-8insT MANE Select	NP_036335.1:n.866-9_866-8insT