Canonical Allele Identifier: CA652908818

Gene: GRHPR

Linked Data

• dbSNP Id: rs1554749626
• COSMIC: COSN17154249

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436642_37436643insCT , CM000671.2:g.37436642_37436643insCT	GRCh38
NC_000009.11:g.37436639_37436640insCT , CM000671.1:g.37436639_37436640insCT	GRCh37
NC_000009.10:g.37426639_37426640insCT	NCBI36
NG_008135.1:g.18933_18934insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-19_866-18insCT MANE Select	ENSP00000313432.6:n.866-19_866-18insCT
ENST00000318158.10:c.866-19_866-18insCT	ENSP00000313432.6:n.866-19_866-18insCT
ENST00000460882.5:n.893-19_893-18insCT
ENST00000480596.5:n.1567-19_1567-18insCT
ENST00000491488.5:n.571-19_571-18insCT
ENST00000494290.1:c.*52-239_*52-238insCT	ENSP00000432021.1:n.*52-239_*52-238insCT
ENST00000497693.1:n.4434-19_4434-18insCT
NM_012203.1:c.866-19_866-18insCT	NP_036335.1:n.866-19_866-18insCT
XM_005251631.1:c.545-19_545-18insCT	XP_005251688.1:n.545-19_545-18insCT
XM_011518073.1:c.464-19_464-18insCT	XP_011516375.1:n.464-19_464-18insCT
XM_017015320.2:c.946-769_946-768insCT	XP_016870809.1:n.946-769_946-768insCT
XM_017015321.2:c.866-769_866-768insCT	XP_016870810.1:n.866-769_866-768insCT
XM_017015323.2:c.544-769_544-768insCT	XP_016870812.1:n.544-769_544-768insCT
XM_024447716.1:c.1219-769_1219-768insCT	XP_024303484.1:n.1219-769_1219-768insCT
XM_024447717.1:c.1139-769_1139-768insCT	XP_024303485.1:n.1139-769_1139-768insCT
XR_002956828.1:n.1234-769_1234-768insCT
XR_002956829.1:n.1154-769_1154-768insCT
XR_002956830.1:n.2286-19_2286-18insCT
XR_002956831.1:n.1961-19_1961-18insCT
XR_002956832.1:n.1285-19_1285-18insCT
NM_012203.2:c.866-19_866-18insCT MANE Select	NP_036335.1:n.866-19_866-18insCT