Canonical Allele Identifier: CA2689984567

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436630-ATCTCCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436635_37436640del , CM000671.2:g.37436635_37436640del	GRCh38
NC_000009.11:g.37436632_37436637del , CM000671.1:g.37436632_37436637del	GRCh37
NC_000009.10:g.37426632_37426637del	NCBI36
NG_008135.1:g.18926_18931del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-26_866-21del MANE Select	ENSP00000313432.6:n.866-26_866-21del
ENST00000318158.10:c.866-26_866-21del	ENSP00000313432.6:n.866-26_866-21del
ENST00000460882.5:n.893-26_893-21del
ENST00000480596.5:n.1567-26_1567-21del
ENST00000491488.5:n.571-26_571-21del
ENST00000494290.1:c.*52-246_*52-241del	ENSP00000432021.1:n.*52-246_*52-241del
ENST00000497693.1:n.4434-26_4434-21del
NM_012203.1:c.866-26_866-21del	NP_036335.1:n.866-26_866-21del
XM_005251631.1:c.545-26_545-21del	XP_005251688.1:n.545-26_545-21del
XM_011518073.1:c.464-26_464-21del	XP_011516375.1:n.464-26_464-21del
XM_017015320.2:c.946-776_946-771del	XP_016870809.1:n.946-776_946-771del
XM_017015321.2:c.866-776_866-771del	XP_016870810.1:n.866-776_866-771del
XM_017015323.2:c.544-776_544-771del	XP_016870812.1:n.544-776_544-771del
XM_024447716.1:c.1219-776_1219-771del	XP_024303484.1:n.1219-776_1219-771del
XM_024447717.1:c.1139-776_1139-771del	XP_024303485.1:n.1139-776_1139-771del
XR_002956828.1:n.1234-776_1234-771del
XR_002956829.1:n.1154-776_1154-771del
XR_002956830.1:n.2286-26_2286-21del
XR_002956831.1:n.1961-26_1961-21del
XR_002956832.1:n.1285-26_1285-21del
NM_012203.2:c.866-26_866-21del MANE Select	NP_036335.1:n.866-26_866-21del