Canonical Allele Identifier: CA2579340804

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436843-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436844_37436845del , CM000671.2:g.37436844_37436845del	GRCh38
NC_000009.11:g.37436841_37436842del , CM000671.1:g.37436841_37436842del	GRCh37
NC_000009.10:g.37426841_37426842del	NCBI36
NG_008135.1:g.19135_19136del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*62_*63del MANE Select	ENSP00000313432.6:n.*62_*63del
ENST00000318158.10:c.*62_*63del	ENSP00000313432.6:n.*62_*63del
ENST00000460882.5:n.1076_1077del
ENST00000480596.5:n.1750_1751del
ENST00000494290.1:c.*52-37_*52-36del	ENSP00000432021.1:n.*52-37_*52-36del
ENST00000497693.1:n.4617_4618del
NM_012203.1:c.*62_*63del	NP_036335.1:n.*62_*63del
XM_005251631.1:c.*62_*63del	XP_005251688.1:n.*62_*63del
XM_011518073.1:c.*62_*63del	XP_011516375.1:n.*62_*63del
XM_017015320.2:c.946-567_946-566del	XP_016870809.1:n.946-567_946-566del
XM_017015321.2:c.866-567_866-566del	XP_016870810.1:n.866-567_866-566del
XM_017015323.2:c.544-567_544-566del	XP_016870812.1:n.544-567_544-566del
XM_024447716.1:c.1219-567_1219-566del	XP_024303484.1:n.1219-567_1219-566del
XM_024447717.1:c.1139-567_1139-566del	XP_024303485.1:n.1139-567_1139-566del
XR_002956828.1:n.1234-567_1234-566del
XR_002956829.1:n.1154-567_1154-566del
XR_002956830.1:n.2469_2470del
XR_002956831.1:n.2144_2145del
XR_002956832.1:n.1468_1469del
NM_012203.2:c.*62_*63del MANE Select	NP_036335.1:n.*62_*63del