Canonical Allele Identifier: CA1846885918

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436758_37436760delinsGAT , CM000671.2:g.37436758_37436760delinsGAT	GRCh38
NC_000009.11:g.37436755_37436757delinsGAT , CM000671.1:g.37436755_37436757delinsGAT	GRCh37
NC_000009.10:g.37426755_37426757delinsGAT	NCBI36
NG_008135.1:g.19049_19051delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.963_965delinsGAT MANE Select	ENSP00000313432.6:p.Pro321=
ENST00000318158.10:c.963_965delinsGAT	ENSP00000313432.6:p.Pro321=
ENST00000460882.5:n.990_992delinsGAT
ENST00000480596.5:n.1664_1666delinsGAT
ENST00000494290.1:c.*52-123_*52-121delinsGAT	ENSP00000432021.1:n.*52-123_*52-121delinsGAT
ENST00000497693.1:n.4531_4533delinsGAT
NM_012203.1:c.963_965delinsGAT	NP_036335.1:p.Pro321=
XM_005251631.1:c.642_644delinsGAT	XP_005251688.1:p.Pro214=
XM_011518073.1:c.561_563delinsGAT	XP_011516375.1:p.Pro187=
XM_017015320.2:c.946-653_946-651delinsGAT	XP_016870809.1:n.946-653_946-651delinsGAT
XM_017015321.2:c.866-653_866-651delinsGAT	XP_016870810.1:n.866-653_866-651delinsGAT
XM_017015323.2:c.544-653_544-651delinsGAT	XP_016870812.1:n.544-653_544-651delinsGAT
XM_024447716.1:c.1219-653_1219-651delinsGAT	XP_024303484.1:n.1219-653_1219-651delinsGAT
XM_024447717.1:c.1139-653_1139-651delinsGAT	XP_024303485.1:n.1139-653_1139-651delinsGAT
XR_002956828.1:n.1234-653_1234-651delinsGAT
XR_002956829.1:n.1154-653_1154-651delinsGAT
XR_002956830.1:n.2383_2385delinsGAT
XR_002956831.1:n.2058_2060delinsGAT
XR_002956832.1:n.1382_1384delinsGAT
NM_012203.2:c.963_965delinsGAT MANE Select	NP_036335.1:p.Pro321=