Canonical Allele Identifier: CA1846864855

Gene: GRHPR

Linked Data

• dbSNP Id: rs1823002401

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37424870_37424877del , CM000671.2:g.37424870_37424877del	GRCh38
NC_000009.11:g.37424867_37424874del , CM000671.1:g.37424867_37424874del	GRCh37
NC_000009.10:g.37414867_37414874del	NCBI36
NG_008135.1:g.7161_7168del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.109_116del MANE Select	ENSP00000313432.6:p.Asp37HisfsTer?
ENST00000318158.10:c.109_116del	ENSP00000313432.6:p.Asp37HisfsTer?
ENST00000377824.8:n.146_153del
ENST00000460882.5:n.136_143del
ENST00000487399.5:n.118_125del
ENST00000491488.5:n.109+2037_109+2044del
ENST00000493368.5:n.166_173del
ENST00000607784.1:c.109_116del	ENSP00000475569.1:p.Asp37HisfsTer?
NM_012203.1:c.109_116del	NP_036335.1:p.Asp37HisfsTer?
XM_005251631.1:c.83+2037_83+2044del	XP_005251688.1:n.83+2037_83+2044del
XM_011518073.1:c.-654_-647del	XP_011516375.1:n.-654_-647del
XR_929374.1:n.194_201del
XM_017015320.2:c.109_116del	XP_016870809.1:p.Asp37HisfsTer?
XM_017015321.2:c.109_116del	XP_016870810.1:p.Asp37HisfsTer?
XM_017015323.2:c.-654_-647del	XP_016870812.1:n.-654_-647del
XM_024447716.1:c.382_389del	XP_024303484.1:p.Asp128HisfsTer?
XM_024447717.1:c.382_389del	XP_024303485.1:p.Asp128HisfsTer?
XR_002956828.1:n.397_404del
XR_002956829.1:n.397_404del
XR_002956830.1:n.168_175del
XR_002956831.1:n.138+2037_138+2044del
XR_002956832.1:n.168_175del
NM_012203.2:c.109_116del MANE Select	NP_036335.1:p.Asp37HisfsTer?