Canonical Allele Identifier: CA2689984591

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436647-TCTCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436650_37436654del , CM000671.2:g.37436650_37436654del	GRCh38
NC_000009.11:g.37436647_37436651del , CM000671.1:g.37436647_37436651del	GRCh37
NC_000009.10:g.37426647_37426651del	NCBI36
NG_008135.1:g.18941_18945del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.866-11_866-7del MANE Select	ENSP00000313432.6:n.866-11_866-7del
ENST00000318158.10:c.866-11_866-7del	ENSP00000313432.6:n.866-11_866-7del
ENST00000460882.5:n.893-11_893-7del
ENST00000480596.5:n.1567-11_1567-7del
ENST00000491488.5:n.571-11_571-7del
ENST00000494290.1:c.*52-231_*52-227del	ENSP00000432021.1:n.*52-231_*52-227del
ENST00000497693.1:n.4434-11_4434-7del
NM_012203.1:c.866-11_866-7del	NP_036335.1:n.866-11_866-7del
XM_005251631.1:c.545-11_545-7del	XP_005251688.1:n.545-11_545-7del
XM_011518073.1:c.464-11_464-7del	XP_011516375.1:n.464-11_464-7del
XM_017015320.2:c.946-761_946-757del	XP_016870809.1:n.946-761_946-757del
XM_017015321.2:c.866-761_866-757del	XP_016870810.1:n.866-761_866-757del
XM_017015323.2:c.544-761_544-757del	XP_016870812.1:n.544-761_544-757del
XM_024447716.1:c.1219-761_1219-757del	XP_024303484.1:n.1219-761_1219-757del
XM_024447717.1:c.1139-761_1139-757del	XP_024303485.1:n.1139-761_1139-757del
XR_002956828.1:n.1234-761_1234-757del
XR_002956829.1:n.1154-761_1154-757del
XR_002956830.1:n.2286-11_2286-7del
XR_002956831.1:n.1961-11_1961-7del
XR_002956832.1:n.1285-11_1285-7del
NM_012203.2:c.866-11_866-7del MANE Select	NP_036335.1:n.866-11_866-7del