Canonical Allele Identifier: CA2689981282

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37429668-ATGCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429669_37429672del , CM000671.2:g.37429669_37429672del	GRCh38
NC_000009.11:g.37429666_37429669del , CM000671.1:g.37429666_37429669del	GRCh37
NC_000009.10:g.37419666_37419669del	NCBI36
NG_008135.1:g.11960_11963del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.494-63_494-60del MANE Select	ENSP00000313432.6:n.494-63_494-60del
ENST00000318158.10:c.494-63_494-60del	ENSP00000313432.6:n.494-63_494-60del
ENST00000377824.8:n.531-63_531-60del
ENST00000460882.5:n.521-63_521-60del
ENST00000480596.5:n.1132_1135del
ENST00000491488.5:n.199-63_199-60del
ENST00000494290.1:c.2_5del	ENSP00000432021.1:p.Met1ArgfsTer20
ENST00000497693.1:n.1964_1967del
ENST00000607784.1:c.494-63_494-60del	ENSP00000475569.1:n.494-63_494-60del
NM_012203.1:c.494-63_494-60del	NP_036335.1:n.494-63_494-60del
XM_005251631.1:c.173-63_173-60del	XP_005251688.1:n.173-63_173-60del
XM_011518073.1:c.92-63_92-60del	XP_011516375.1:n.92-63_92-60del
XR_929374.1:n.939-63_939-60del
XM_017015320.2:c.494-63_494-60del	XP_016870809.1:n.494-63_494-60del
XM_017015321.2:c.494-63_494-60del	XP_016870810.1:n.494-63_494-60del
XM_017015323.2:c.92-63_92-60del	XP_016870812.1:n.92-63_92-60del
XM_024447716.1:c.767-63_767-60del	XP_024303484.1:n.767-63_767-60del
XM_024447717.1:c.767-63_767-60del	XP_024303485.1:n.767-63_767-60del
XR_002956828.1:n.782-63_782-60del
XR_002956829.1:n.782-63_782-60del
XR_002956830.1:n.553-63_553-60del
XR_002956831.1:n.228-63_228-60del
XR_002956832.1:n.913-63_913-60del
NM_012203.2:c.494-63_494-60del MANE Select	NP_036335.1:n.494-63_494-60del