Canonical Allele Identifier: CA2783586319

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436632_37436633insCT , CM000671.2:g.37436632_37436633insCT	GRCh38
NC_000009.11:g.37436629_37436630insCT , CM000671.1:g.37436629_37436630insCT	GRCh37
NC_000009.10:g.37426629_37426630insCT	NCBI36
NG_008135.1:g.18923_18924insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-29_866-28insCT MANE Select	ENSP00000313432.6:n.866-29_866-28insCT
ENST00000318158.10:c.866-29_866-28insCT	ENSP00000313432.6:n.866-29_866-28insCT
ENST00000460882.5:n.893-29_893-28insCT
ENST00000480596.5:n.1567-29_1567-28insCT
ENST00000491488.5:n.571-29_571-28insCT
ENST00000494290.1:c.*52-249_*52-248insCT	ENSP00000432021.1:n.*52-249_*52-248insCT
ENST00000497693.1:n.4434-29_4434-28insCT
NM_012203.1:c.866-29_866-28insCT	NP_036335.1:n.866-29_866-28insCT
XM_005251631.1:c.545-29_545-28insCT	XP_005251688.1:n.545-29_545-28insCT
XM_011518073.1:c.464-29_464-28insCT	XP_011516375.1:n.464-29_464-28insCT
XM_017015320.2:c.946-779_946-778insCT	XP_016870809.1:n.946-779_946-778insCT
XM_017015321.2:c.866-779_866-778insCT	XP_016870810.1:n.866-779_866-778insCT
XM_017015323.2:c.544-779_544-778insCT	XP_016870812.1:n.544-779_544-778insCT
XM_024447716.1:c.1219-779_1219-778insCT	XP_024303484.1:n.1219-779_1219-778insCT
XM_024447717.1:c.1139-779_1139-778insCT	XP_024303485.1:n.1139-779_1139-778insCT
XR_002956828.1:n.1234-779_1234-778insCT
XR_002956829.1:n.1154-779_1154-778insCT
XR_002956830.1:n.2286-29_2286-28insCT
XR_002956831.1:n.1961-29_1961-28insCT
XR_002956832.1:n.1285-29_1285-28insCT
NM_012203.2:c.866-29_866-28insCT MANE Select	NP_036335.1:n.866-29_866-28insCT