Canonical Allele Identifier: CA1846885132

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436557_37436561delinsCTCTT , CM000671.2:g.37436557_37436561delinsCTCTT	GRCh38
NC_000009.11:g.37436554_37436558delinsCTCTT , CM000671.1:g.37436554_37436558delinsCTCTT	GRCh37
NC_000009.10:g.37426554_37426558delinsCTCTT	NCBI36
NG_008135.1:g.18848_18852delinsCTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-104_866-100delinsCTCTT MANE Select	ENSP00000313432.6:n.866-104_866-100delinsCTCTT
ENST00000318158.10:c.866-104_866-100delinsCTCTT	ENSP00000313432.6:n.866-104_866-100delinsCTCTT
ENST00000460882.5:n.893-104_893-100delinsCTCTT
ENST00000480596.5:n.1567-104_1567-100delinsCTCTT
ENST00000491488.5:n.571-104_571-100delinsCTCTT
ENST00000494290.1:c.*52-324_*52-320delinsCTCTT	ENSP00000432021.1:n.*52-324_*52-320delinsCTCTT
ENST00000497693.1:n.4434-104_4434-100delinsCTCTT
NM_012203.1:c.866-104_866-100delinsCTCTT	NP_036335.1:n.866-104_866-100delinsCTCTT
XM_005251631.1:c.545-104_545-100delinsCTCTT	XP_005251688.1:n.545-104_545-100delinsCTCTT
XM_011518073.1:c.464-104_464-100delinsCTCTT	XP_011516375.1:n.464-104_464-100delinsCTCTT
XM_017015320.2:c.946-854_946-850delinsCTCTT	XP_016870809.1:n.946-854_946-850delinsCTCTT
XM_017015321.2:c.866-854_866-850delinsCTCTT	XP_016870810.1:n.866-854_866-850delinsCTCTT
XM_017015323.2:c.544-854_544-850delinsCTCTT	XP_016870812.1:n.544-854_544-850delinsCTCTT
XM_024447716.1:c.1219-854_1219-850delinsCTCTT	XP_024303484.1:n.1219-854_1219-850delinsCTCTT
XM_024447717.1:c.1139-854_1139-850delinsCTCTT	XP_024303485.1:n.1139-854_1139-850delinsCTCTT
XR_002956828.1:n.1234-854_1234-850delinsCTCTT
XR_002956829.1:n.1154-854_1154-850delinsCTCTT
XR_002956830.1:n.2286-104_2286-100delinsCTCTT
XR_002956831.1:n.1961-104_1961-100delinsCTCTT
XR_002956832.1:n.1285-104_1285-100delinsCTCTT
NM_012203.2:c.866-104_866-100delinsCTCTT MANE Select	NP_036335.1:n.866-104_866-100delinsCTCTT