Canonical Allele Identifier: CA2689981353

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37429860-AGGAGCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429861_37429866del , CM000671.2:g.37429861_37429866del	GRCh38
NC_000009.11:g.37429858_37429863del , CM000671.1:g.37429858_37429863del	GRCh37
NC_000009.10:g.37419858_37419863del	NCBI36
NG_008135.1:g.12152_12157del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.598+25_598+30del MANE Select	ENSP00000313432.6:n.598+25_598+30del
ENST00000318158.10:c.598+25_598+30del	ENSP00000313432.6:n.598+25_598+30del
ENST00000377824.8:n.635+25_635+30del
ENST00000460882.5:n.625+25_625+30del
ENST00000480596.5:n.1299+25_1299+30del
ENST00000482603.1:n.51+25_51+30del
ENST00000491488.5:n.303+25_303+30del
ENST00000494290.1:c.169+25_169+30del	ENSP00000432021.1:n.169+25_169+30del
ENST00000497693.1:n.2156_2161del
ENST00000607784.1:c.598+25_598+30del	ENSP00000475569.1:n.598+25_598+30del
NM_012203.1:c.598+25_598+30del	NP_036335.1:n.598+25_598+30del
XM_005251631.1:c.277+25_277+30del	XP_005251688.1:n.277+25_277+30del
XM_011518073.1:c.196+25_196+30del	XP_011516375.1:n.196+25_196+30del
XR_929374.1:n.1043+25_1043+30del
XM_017015320.2:c.598+25_598+30del	XP_016870809.1:n.598+25_598+30del
XM_017015321.2:c.598+25_598+30del	XP_016870810.1:n.598+25_598+30del
XM_017015323.2:c.196+25_196+30del	XP_016870812.1:n.196+25_196+30del
XM_024447716.1:c.871+25_871+30del	XP_024303484.1:n.871+25_871+30del
XM_024447717.1:c.871+25_871+30del	XP_024303485.1:n.871+25_871+30del
XR_002956828.1:n.886+25_886+30del
XR_002956829.1:n.886+25_886+30del
XR_002956830.1:n.657+25_657+30del
XR_002956831.1:n.332+25_332+30del
XR_002956832.1:n.1017+25_1017+30del
NM_012203.2:c.598+25_598+30del MANE Select	NP_036335.1:n.598+25_598+30del