Canonical Allele Identifier: CA1846885135

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436559_37436561delinsCTT , CM000671.2:g.37436559_37436561delinsCTT	GRCh38
NC_000009.11:g.37436556_37436558delinsCTT , CM000671.1:g.37436556_37436558delinsCTT	GRCh37
NC_000009.10:g.37426556_37426558delinsCTT	NCBI36
NG_008135.1:g.18850_18852delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-102_866-100delinsCTT MANE Select	ENSP00000313432.6:n.866-102_866-100delinsCTT
ENST00000318158.10:c.866-102_866-100delinsCTT	ENSP00000313432.6:n.866-102_866-100delinsCTT
ENST00000460882.5:n.893-102_893-100delinsCTT
ENST00000480596.5:n.1567-102_1567-100delinsCTT
ENST00000491488.5:n.571-102_571-100delinsCTT
ENST00000494290.1:c.*52-322_*52-320delinsCTT	ENSP00000432021.1:n.*52-322_*52-320delinsCTT
ENST00000497693.1:n.4434-102_4434-100delinsCTT
NM_012203.1:c.866-102_866-100delinsCTT	NP_036335.1:n.866-102_866-100delinsCTT
XM_005251631.1:c.545-102_545-100delinsCTT	XP_005251688.1:n.545-102_545-100delinsCTT
XM_011518073.1:c.464-102_464-100delinsCTT	XP_011516375.1:n.464-102_464-100delinsCTT
XM_017015320.2:c.946-852_946-850delinsCTT	XP_016870809.1:n.946-852_946-850delinsCTT
XM_017015321.2:c.866-852_866-850delinsCTT	XP_016870810.1:n.866-852_866-850delinsCTT
XM_017015323.2:c.544-852_544-850delinsCTT	XP_016870812.1:n.544-852_544-850delinsCTT
XM_024447716.1:c.1219-852_1219-850delinsCTT	XP_024303484.1:n.1219-852_1219-850delinsCTT
XM_024447717.1:c.1139-852_1139-850delinsCTT	XP_024303485.1:n.1139-852_1139-850delinsCTT
XR_002956828.1:n.1234-852_1234-850delinsCTT
XR_002956829.1:n.1154-852_1154-850delinsCTT
XR_002956830.1:n.2286-102_2286-100delinsCTT
XR_002956831.1:n.1961-102_1961-100delinsCTT
XR_002956832.1:n.1285-102_1285-100delinsCTT
NM_012203.2:c.866-102_866-100delinsCTT MANE Select	NP_036335.1:n.866-102_866-100delinsCTT