Canonical Allele Identifier: CA2842782205

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37424918dup , CM000671.2:g.37424918dup	GRCh38
NC_000009.11:g.37424915dup , CM000671.1:g.37424915dup	GRCh37
NC_000009.10:g.37414915dup	NCBI36
NG_008135.1:g.7209dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.157dup MANE Select	ENSP00000313432.6:p.His53ProfsTer?
ENST00000318158.10:c.157dup	ENSP00000313432.6:p.His53ProfsTer?
ENST00000377824.8:n.194dup
ENST00000460882.5:n.184dup
ENST00000487399.5:n.166dup
ENST00000491488.5:n.109+2085dup
ENST00000493368.5:n.214dup
ENST00000607784.1:c.157dup	ENSP00000475569.1:p.His53ProfsTer?
NM_012203.1:c.157dup	NP_036335.1:p.His53ProfsTer?
XM_005251631.1:c.83+2085dup	XP_005251688.1:n.83+2085dup
XM_011518073.1:c.-606dup	XP_011516375.1:n.-606dup
XR_929374.1:n.242dup
XM_017015320.2:c.157dup	XP_016870809.1:p.His53ProfsTer?
XM_017015321.2:c.157dup	XP_016870810.1:p.His53ProfsTer?
XM_017015323.2:c.-606dup	XP_016870812.1:n.-606dup
XM_024447716.1:c.430dup	XP_024303484.1:p.His144ProfsTer?
XM_024447717.1:c.430dup	XP_024303485.1:p.His144ProfsTer?
XR_002956828.1:n.445dup
XR_002956829.1:n.445dup
XR_002956830.1:n.216dup
XR_002956831.1:n.138+2085dup
XR_002956832.1:n.216dup
NM_012203.2:c.157dup MANE Select	NP_036335.1:p.His53ProfsTer?