Canonical Allele Identifier: CA2689984572

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436634-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436634_37436635insT , CM000671.2:g.37436634_37436635insT	GRCh38
NC_000009.11:g.37436631_37436632insT , CM000671.1:g.37436631_37436632insT	GRCh37
NC_000009.10:g.37426631_37426632insT	NCBI36
NG_008135.1:g.18925_18926insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-27_866-26insT MANE Select	ENSP00000313432.6:n.866-27_866-26insT
ENST00000318158.10:c.866-27_866-26insT	ENSP00000313432.6:n.866-27_866-26insT
ENST00000460882.5:n.893-27_893-26insT
ENST00000480596.5:n.1567-27_1567-26insT
ENST00000491488.5:n.571-27_571-26insT
ENST00000494290.1:c.*52-247_*52-246insT	ENSP00000432021.1:n.*52-247_*52-246insT
ENST00000497693.1:n.4434-27_4434-26insT
NM_012203.1:c.866-27_866-26insT	NP_036335.1:n.866-27_866-26insT
XM_005251631.1:c.545-27_545-26insT	XP_005251688.1:n.545-27_545-26insT
XM_011518073.1:c.464-27_464-26insT	XP_011516375.1:n.464-27_464-26insT
XM_017015320.2:c.946-777_946-776insT	XP_016870809.1:n.946-777_946-776insT
XM_017015321.2:c.866-777_866-776insT	XP_016870810.1:n.866-777_866-776insT
XM_017015323.2:c.544-777_544-776insT	XP_016870812.1:n.544-777_544-776insT
XM_024447716.1:c.1219-777_1219-776insT	XP_024303484.1:n.1219-777_1219-776insT
XM_024447717.1:c.1139-777_1139-776insT	XP_024303485.1:n.1139-777_1139-776insT
XR_002956828.1:n.1234-777_1234-776insT
XR_002956829.1:n.1154-777_1154-776insT
XR_002956830.1:n.2286-27_2286-26insT
XR_002956831.1:n.1961-27_1961-26insT
XR_002956832.1:n.1285-27_1285-26insT
NM_012203.2:c.866-27_866-26insT MANE Select	NP_036335.1:n.866-27_866-26insT