Canonical Allele Identifier: CA2689984592

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436647-TCTCTCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436648_37436653del , CM000671.2:g.37436648_37436653del	GRCh38
NC_000009.11:g.37436645_37436650del , CM000671.1:g.37436645_37436650del	GRCh37
NC_000009.10:g.37426645_37426650del	NCBI36
NG_008135.1:g.18939_18944del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.866-13_866-8del MANE Select	ENSP00000313432.6:n.866-13_866-8del
ENST00000318158.10:c.866-13_866-8del	ENSP00000313432.6:n.866-13_866-8del
ENST00000460882.5:n.893-13_893-8del
ENST00000480596.5:n.1567-13_1567-8del
ENST00000491488.5:n.571-13_571-8del
ENST00000494290.1:c.*52-233_*52-228del	ENSP00000432021.1:n.*52-233_*52-228del
ENST00000497693.1:n.4434-13_4434-8del
NM_012203.1:c.866-13_866-8del	NP_036335.1:n.866-13_866-8del
XM_005251631.1:c.545-13_545-8del	XP_005251688.1:n.545-13_545-8del
XM_011518073.1:c.464-13_464-8del	XP_011516375.1:n.464-13_464-8del
XM_017015320.2:c.946-763_946-758del	XP_016870809.1:n.946-763_946-758del
XM_017015321.2:c.866-763_866-758del	XP_016870810.1:n.866-763_866-758del
XM_017015323.2:c.544-763_544-758del	XP_016870812.1:n.544-763_544-758del
XM_024447716.1:c.1219-763_1219-758del	XP_024303484.1:n.1219-763_1219-758del
XM_024447717.1:c.1139-763_1139-758del	XP_024303485.1:n.1139-763_1139-758del
XR_002956828.1:n.1234-763_1234-758del
XR_002956829.1:n.1154-763_1154-758del
XR_002956830.1:n.2286-13_2286-8del
XR_002956831.1:n.1961-13_1961-8del
XR_002956832.1:n.1285-13_1285-8del
NM_012203.2:c.866-13_866-8del MANE Select	NP_036335.1:n.866-13_866-8del