Canonical Allele Identifier: CA2838955231

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37424941dup , CM000671.2:g.37424941dup	GRCh38
NC_000009.11:g.37424938dup , CM000671.1:g.37424938dup	GRCh37
NC_000009.10:g.37414938dup	NCBI36
NG_008135.1:g.7232dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.180dup MANE Select	ENSP00000313432.6:p.Asp61ArgfsTer?
ENST00000318158.10:c.180dup	ENSP00000313432.6:p.Asp61ArgfsTer?
ENST00000377824.8:n.217dup
ENST00000460882.5:n.207dup
ENST00000487399.5:n.189dup
ENST00000491488.5:n.109+2108dup
ENST00000493368.5:n.237dup
ENST00000607784.1:c.180dup	ENSP00000475569.1:p.Asp61ArgfsTer?
NM_012203.1:c.180dup	NP_036335.1:p.Asp61ArgfsTer?
XM_005251631.1:c.83+2108dup	XP_005251688.1:n.83+2108dup
XM_011518073.1:c.-583dup	XP_011516375.1:n.-583dup
XR_929374.1:n.265dup
XM_017015320.2:c.180dup	XP_016870809.1:p.Asp61ArgfsTer?
XM_017015321.2:c.180dup	XP_016870810.1:p.Asp61ArgfsTer?
XM_017015323.2:c.-583dup	XP_016870812.1:n.-583dup
XM_024447716.1:c.453dup	XP_024303484.1:p.Asp152ArgfsTer?
XM_024447717.1:c.453dup	XP_024303485.1:p.Asp152ArgfsTer?
XR_002956828.1:n.468dup
XR_002956829.1:n.468dup
XR_002956830.1:n.239dup
XR_002956831.1:n.138+2108dup
XR_002956832.1:n.239dup
NM_012203.2:c.180dup MANE Select	NP_036335.1:p.Asp61ArgfsTer?