Canonical Allele Identifier: CA2689981089

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37429494-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429497_37429498del , CM000671.2:g.37429497_37429498del	GRCh38
NC_000009.11:g.37429494_37429495del , CM000671.1:g.37429494_37429495del	GRCh37
NC_000009.10:g.37419494_37419495del	NCBI36
NG_008135.1:g.11788_11789del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.494-235_494-234del MANE Select	ENSP00000313432.6:n.494-235_494-234del
ENST00000318158.10:c.494-235_494-234del	ENSP00000313432.6:n.494-235_494-234del
ENST00000377824.8:n.531-235_531-234del
ENST00000460882.5:n.521-235_521-234del
ENST00000480596.5:n.960_961del
ENST00000491488.5:n.199-235_199-234del
ENST00000494290.1:c.-171_-170del	ENSP00000432021.1:n.-171_-170del
ENST00000497693.1:n.1792_1793del
ENST00000607784.1:c.494-235_494-234del	ENSP00000475569.1:n.494-235_494-234del
NM_012203.1:c.494-235_494-234del	NP_036335.1:n.494-235_494-234del
XM_005251631.1:c.173-235_173-234del	XP_005251688.1:n.173-235_173-234del
XM_011518073.1:c.92-235_92-234del	XP_011516375.1:n.92-235_92-234del
XR_929374.1:n.939-235_939-234del
XM_017015320.2:c.494-235_494-234del	XP_016870809.1:n.494-235_494-234del
XM_017015321.2:c.494-235_494-234del	XP_016870810.1:n.494-235_494-234del
XM_017015323.2:c.92-235_92-234del	XP_016870812.1:n.92-235_92-234del
XM_024447716.1:c.767-235_767-234del	XP_024303484.1:n.767-235_767-234del
XM_024447717.1:c.767-235_767-234del	XP_024303485.1:n.767-235_767-234del
XR_002956828.1:n.782-235_782-234del
XR_002956829.1:n.782-235_782-234del
XR_002956830.1:n.553-235_553-234del
XR_002956831.1:n.228-235_228-234del
XR_002956832.1:n.913-235_913-234del
NM_012203.2:c.494-235_494-234del MANE Select	NP_036335.1:n.494-235_494-234del