Canonical Allele Identifier: CA1846864875

Gene: GRHPR

Linked Data

• dbSNP Id: rs1823003304

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37424879_37424880insC , CM000671.2:g.37424879_37424880insC	GRCh38
NC_000009.11:g.37424876_37424877insC , CM000671.1:g.37424876_37424877insC	GRCh37
NC_000009.10:g.37414876_37414877insC	NCBI36
NG_008135.1:g.7170_7171insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.118_119insC MANE Select	ENSP00000313432.6:p.Ile40ThrfsTer?
ENST00000318158.10:c.118_119insC	ENSP00000313432.6:p.Ile40ThrfsTer?
ENST00000377824.8:n.155_156insC
ENST00000460882.5:n.145_146insC
ENST00000487399.5:n.127_128insC
ENST00000491488.5:n.109+2046_109+2047insC
ENST00000493368.5:n.175_176insC
ENST00000607784.1:c.118_119insC	ENSP00000475569.1:p.Ile40ThrfsTer?
NM_012203.1:c.118_119insC	NP_036335.1:p.Ile40ThrfsTer?
XM_005251631.1:c.83+2046_83+2047insC	XP_005251688.1:n.83+2046_83+2047insC
XM_011518073.1:c.-645_-644insC	XP_011516375.1:n.-645_-644insC
XR_929374.1:n.203_204insC
XM_017015320.2:c.118_119insC	XP_016870809.1:p.Ile40ThrfsTer?
XM_017015321.2:c.118_119insC	XP_016870810.1:p.Ile40ThrfsTer?
XM_017015323.2:c.-645_-644insC	XP_016870812.1:n.-645_-644insC
XM_024447716.1:c.391_392insC	XP_024303484.1:p.Ile131ThrfsTer?
XM_024447717.1:c.391_392insC	XP_024303485.1:p.Ile131ThrfsTer?
XR_002956828.1:n.406_407insC
XR_002956829.1:n.406_407insC
XR_002956830.1:n.177_178insC
XR_002956831.1:n.138+2046_138+2047insC
XR_002956832.1:n.177_178insC
NM_012203.2:c.118_119insC MANE Select	NP_036335.1:p.Ile40ThrfsTer?