Canonical Allele Identifier: CA2689981168

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37429553-TGGGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429555_37429558del , CM000671.2:g.37429555_37429558del	GRCh38
NC_000009.11:g.37429552_37429555del , CM000671.1:g.37429552_37429555del	GRCh37
NC_000009.10:g.37419552_37419555del	NCBI36
NG_008135.1:g.11846_11849del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.494-177_494-174del MANE Select	ENSP00000313432.6:n.494-177_494-174del
ENST00000318158.10:c.494-177_494-174del	ENSP00000313432.6:n.494-177_494-174del
ENST00000377824.8:n.531-177_531-174del
ENST00000460882.5:n.521-177_521-174del
ENST00000480596.5:n.1018_1021del
ENST00000491488.5:n.199-177_199-174del
ENST00000494290.1:c.-113_-110del	ENSP00000432021.1:n.-113_-110del
ENST00000497693.1:n.1850_1853del
ENST00000607784.1:c.494-177_494-174del	ENSP00000475569.1:n.494-177_494-174del
NM_012203.1:c.494-177_494-174del	NP_036335.1:n.494-177_494-174del
XM_005251631.1:c.173-177_173-174del	XP_005251688.1:n.173-177_173-174del
XM_011518073.1:c.92-177_92-174del	XP_011516375.1:n.92-177_92-174del
XR_929374.1:n.939-177_939-174del
XM_017015320.2:c.494-177_494-174del	XP_016870809.1:n.494-177_494-174del
XM_017015321.2:c.494-177_494-174del	XP_016870810.1:n.494-177_494-174del
XM_017015323.2:c.92-177_92-174del	XP_016870812.1:n.92-177_92-174del
XM_024447716.1:c.767-177_767-174del	XP_024303484.1:n.767-177_767-174del
XM_024447717.1:c.767-177_767-174del	XP_024303485.1:n.767-177_767-174del
XR_002956828.1:n.782-177_782-174del
XR_002956829.1:n.782-177_782-174del
XR_002956830.1:n.553-177_553-174del
XR_002956831.1:n.228-177_228-174del
XR_002956832.1:n.913-177_913-174del
NM_012203.2:c.494-177_494-174del MANE Select	NP_036335.1:n.494-177_494-174del