Canonical Allele Identifier: CA2689981287

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37429673-GGGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429678_37429680del , CM000671.2:g.37429678_37429680del	GRCh38
NC_000009.11:g.37429675_37429677del , CM000671.1:g.37429675_37429677del	GRCh37
NC_000009.10:g.37419675_37419677del	NCBI36
NG_008135.1:g.11969_11971del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.494-54_494-52del MANE Select	ENSP00000313432.6:n.494-54_494-52del
ENST00000318158.10:c.494-54_494-52del	ENSP00000313432.6:n.494-54_494-52del
ENST00000377824.8:n.531-54_531-52del
ENST00000460882.5:n.521-54_521-52del
ENST00000480596.5:n.1141_1143del
ENST00000491488.5:n.199-54_199-52del
ENST00000494290.1:c.11_13del	ENSP00000432021.1:p.Gly4del
ENST00000497693.1:n.1973_1975del
ENST00000607784.1:c.494-54_494-52del	ENSP00000475569.1:n.494-54_494-52del
NM_012203.1:c.494-54_494-52del	NP_036335.1:n.494-54_494-52del
XM_005251631.1:c.173-54_173-52del	XP_005251688.1:n.173-54_173-52del
XM_011518073.1:c.92-54_92-52del	XP_011516375.1:n.92-54_92-52del
XR_929374.1:n.939-54_939-52del
XM_017015320.2:c.494-54_494-52del	XP_016870809.1:n.494-54_494-52del
XM_017015321.2:c.494-54_494-52del	XP_016870810.1:n.494-54_494-52del
XM_017015323.2:c.92-54_92-52del	XP_016870812.1:n.92-54_92-52del
XM_024447716.1:c.767-54_767-52del	XP_024303484.1:n.767-54_767-52del
XM_024447717.1:c.767-54_767-52del	XP_024303485.1:n.767-54_767-52del
XR_002956828.1:n.782-54_782-52del
XR_002956829.1:n.782-54_782-52del
XR_002956830.1:n.553-54_553-52del
XR_002956831.1:n.228-54_228-52del
XR_002956832.1:n.913-54_913-52del
NM_012203.2:c.494-54_494-52del MANE Select	NP_036335.1:n.494-54_494-52del