Canonical Allele Identifier: CA2689984485

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436509-TTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436510_37436511del , CM000671.2:g.37436510_37436511del	GRCh38
NC_000009.11:g.37436507_37436508del , CM000671.1:g.37436507_37436508del	GRCh37
NC_000009.10:g.37426507_37426508del	NCBI36
NG_008135.1:g.18801_18802del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-151_866-150del MANE Select	ENSP00000313432.6:n.866-151_866-150del
ENST00000318158.10:c.866-151_866-150del	ENSP00000313432.6:n.866-151_866-150del
ENST00000460882.5:n.893-151_893-150del
ENST00000480596.5:n.1567-151_1567-150del
ENST00000491488.5:n.571-151_571-150del
ENST00000494290.1:c.*52-371_*52-370del	ENSP00000432021.1:n.*52-371_*52-370del
ENST00000497693.1:n.4434-151_4434-150del
NM_012203.1:c.866-151_866-150del	NP_036335.1:n.866-151_866-150del
XM_005251631.1:c.545-151_545-150del	XP_005251688.1:n.545-151_545-150del
XM_011518073.1:c.464-151_464-150del	XP_011516375.1:n.464-151_464-150del
XM_017015320.2:c.946-901_946-900del	XP_016870809.1:n.946-901_946-900del
XM_017015321.2:c.866-901_866-900del	XP_016870810.1:n.866-901_866-900del
XM_017015323.2:c.544-901_544-900del	XP_016870812.1:n.544-901_544-900del
XM_024447716.1:c.1219-901_1219-900del	XP_024303484.1:n.1219-901_1219-900del
XM_024447717.1:c.1139-901_1139-900del	XP_024303485.1:n.1139-901_1139-900del
XR_002956828.1:n.1234-901_1234-900del
XR_002956829.1:n.1154-901_1154-900del
XR_002956830.1:n.2286-151_2286-150del
XR_002956831.1:n.1961-151_1961-150del
XR_002956832.1:n.1285-151_1285-150del
NM_012203.2:c.866-151_866-150del MANE Select	NP_036335.1:n.866-151_866-150del