Canonical Allele Identifier: CA2783586071

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428336_37428337insT , CM000671.2:g.37428336_37428337insT	GRCh38
NC_000009.11:g.37428333_37428334insT , CM000671.1:g.37428333_37428334insT	GRCh37
NC_000009.10:g.37418333_37418334insT	NCBI36
NG_008135.1:g.10627_10628insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.405-148_405-147insT MANE Select	ENSP00000313432.6:n.405-148_405-147insT
ENST00000318158.10:c.405-148_405-147insT	ENSP00000313432.6:n.405-148_405-147insT
ENST00000377824.8:n.442-148_442-147insT
ENST00000460882.5:n.432-148_432-147insT
ENST00000491488.5:n.110-148_110-147insT
ENST00000493368.5:n.462-148_462-147insT
ENST00000497693.1:n.631_632insT
ENST00000607784.1:c.405-148_405-147insT	ENSP00000475569.1:n.405-148_405-147insT
NM_012203.1:c.405-148_405-147insT	NP_036335.1:n.405-148_405-147insT
XM_005251631.1:c.84-148_84-147insT	XP_005251688.1:n.84-148_84-147insT
XM_011518073.1:c.-358-148_-358-147insT	XP_011516375.1:n.-358-148_-358-147insT
XR_929374.1:n.490-148_490-147insT
XM_017015320.2:c.405-148_405-147insT	XP_016870809.1:n.405-148_405-147insT
XM_017015321.2:c.405-148_405-147insT	XP_016870810.1:n.405-148_405-147insT
XM_017015323.2:c.-358-148_-358-147insT	XP_016870812.1:n.-358-148_-358-147insT
XM_024447716.1:c.678-148_678-147insT	XP_024303484.1:n.678-148_678-147insT
XM_024447717.1:c.678-148_678-147insT	XP_024303485.1:n.678-148_678-147insT
XR_002956828.1:n.693-148_693-147insT
XR_002956829.1:n.693-148_693-147insT
XR_002956830.1:n.464-148_464-147insT
XR_002956831.1:n.139-148_139-147insT
XR_002956832.1:n.464-148_464-147insT
NM_012203.2:c.405-148_405-147insT MANE Select	NP_036335.1:n.405-148_405-147insT