Canonical Allele Identifier: CA2689984616

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436835-GAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436840_37436841del , CM000671.2:g.37436840_37436841del	GRCh38
NC_000009.11:g.37436837_37436838del , CM000671.1:g.37436837_37436838del	GRCh37
NC_000009.10:g.37426837_37426838del	NCBI36
NG_008135.1:g.19131_19132del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*58_*59del MANE Select	ENSP00000313432.6:n.*58_*59del
ENST00000318158.10:c.*58_*59del	ENSP00000313432.6:n.*58_*59del
ENST00000460882.5:n.1072_1073del
ENST00000480596.5:n.1746_1747del
ENST00000494290.1:c.*52-41_*52-40del	ENSP00000432021.1:n.*52-41_*52-40del
ENST00000497693.1:n.4613_4614del
NM_012203.1:c.*58_*59del	NP_036335.1:n.*58_*59del
XM_005251631.1:c.*58_*59del	XP_005251688.1:n.*58_*59del
XM_011518073.1:c.*58_*59del	XP_011516375.1:n.*58_*59del
XM_017015320.2:c.946-571_946-570del	XP_016870809.1:n.946-571_946-570del
XM_017015321.2:c.866-571_866-570del	XP_016870810.1:n.866-571_866-570del
XM_017015323.2:c.544-571_544-570del	XP_016870812.1:n.544-571_544-570del
XM_024447716.1:c.1219-571_1219-570del	XP_024303484.1:n.1219-571_1219-570del
XM_024447717.1:c.1139-571_1139-570del	XP_024303485.1:n.1139-571_1139-570del
XR_002956828.1:n.1234-571_1234-570del
XR_002956829.1:n.1154-571_1154-570del
XR_002956830.1:n.2465_2466del
XR_002956831.1:n.2140_2141del
XR_002956832.1:n.1464_1465del
NM_012203.2:c.*58_*59del MANE Select	NP_036335.1:n.*58_*59del