Canonical Allele Identifier: CA1846870605

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429825_37429826delinsAG , CM000671.2:g.37429825_37429826delinsAG	GRCh38
NC_000009.11:g.37429822_37429823delinsAG , CM000671.1:g.37429822_37429823delinsAG	GRCh37
NC_000009.10:g.37419822_37419823delinsAG	NCBI36
NG_008135.1:g.12116_12117delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.587_588delinsAG MANE Select	ENSP00000313432.6:p.Gln196=
ENST00000318158.10:c.587_588delinsAG	ENSP00000313432.6:p.Gln196=
ENST00000377824.8:n.624_625delinsAG
ENST00000460882.5:n.614_615delinsAG
ENST00000480596.5:n.1288_1289delinsAG
ENST00000482603.1:n.40_41delinsAG
ENST00000491488.5:n.292_293delinsAG
ENST00000494290.1:c.158_159delinsAG	ENSP00000432021.1:p.Gln53=
ENST00000497693.1:n.2120_2121delinsAG
ENST00000607784.1:c.587_588delinsAG	ENSP00000475569.1:p.Gln196=
NM_012203.1:c.587_588delinsAG	NP_036335.1:p.Gln196=
XM_005251631.1:c.266_267delinsAG	XP_005251688.1:p.Gln89=
XM_011518073.1:c.185_186delinsAG	XP_011516375.1:p.Gln62=
XR_929374.1:n.1032_1033delinsAG
XM_017015320.2:c.587_588delinsAG	XP_016870809.1:p.Gln196=
XM_017015321.2:c.587_588delinsAG	XP_016870810.1:p.Gln196=
XM_017015323.2:c.185_186delinsAG	XP_016870812.1:p.Gln62=
XM_024447716.1:c.860_861delinsAG	XP_024303484.1:p.Gln287=
XM_024447717.1:c.860_861delinsAG	XP_024303485.1:p.Gln287=
XR_002956828.1:n.875_876delinsAG
XR_002956829.1:n.875_876delinsAG
XR_002956830.1:n.646_647delinsAG
XR_002956831.1:n.321_322delinsAG
XR_002956832.1:n.1006_1007delinsAG
NM_012203.2:c.587_588delinsAG MANE Select	NP_036335.1:p.Gln196=