Canonical Allele Identifier: CA1846864927

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37424910_37424911delinsCG , CM000671.2:g.37424910_37424911delinsCG	GRCh38
NC_000009.11:g.37424907_37424908delinsCG , CM000671.1:g.37424907_37424908delinsCG	GRCh37
NC_000009.10:g.37414907_37414908delinsCG	NCBI36
NG_008135.1:g.7201_7202delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.149_150delinsCG MANE Select	ENSP00000313432.6:p.Ala50=
ENST00000318158.10:c.149_150delinsCG	ENSP00000313432.6:p.Ala50=
ENST00000377824.8:n.186_187delinsCG
ENST00000460882.5:n.176_177delinsCG
ENST00000487399.5:n.158_159delinsCG
ENST00000491488.5:n.109+2077_109+2078delinsCG
ENST00000493368.5:n.206_207delinsCG
ENST00000607784.1:c.149_150delinsCG	ENSP00000475569.1:p.Ala50=
NM_012203.1:c.149_150delinsCG	NP_036335.1:p.Ala50=
XM_005251631.1:c.83+2077_83+2078delinsCG	XP_005251688.1:n.83+2077_83+2078delinsCG
XM_011518073.1:c.-614_-613delinsCG	XP_011516375.1:n.-614_-613delinsCG
XR_929374.1:n.234_235delinsCG
XM_017015320.2:c.149_150delinsCG	XP_016870809.1:p.Ala50=
XM_017015321.2:c.149_150delinsCG	XP_016870810.1:p.Ala50=
XM_017015323.2:c.-614_-613delinsCG	XP_016870812.1:n.-614_-613delinsCG
XM_024447716.1:c.422_423delinsCG	XP_024303484.1:p.Ala141=
XM_024447717.1:c.422_423delinsCG	XP_024303485.1:p.Ala141=
XR_002956828.1:n.437_438delinsCG
XR_002956829.1:n.437_438delinsCG
XR_002956830.1:n.208_209delinsCG
XR_002956831.1:n.138+2077_138+2078delinsCG
XR_002956832.1:n.208_209delinsCG
NM_012203.2:c.149_150delinsCG MANE Select	NP_036335.1:p.Ala50=