Canonical Allele Identifier: CA1846885305

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436624_37436629delinsCTTCTT , CM000671.2:g.37436624_37436629delinsCTTCTT	GRCh38
NC_000009.11:g.37436621_37436626delinsCTTCTT , CM000671.1:g.37436621_37436626delinsCTTCTT	GRCh37
NC_000009.10:g.37426621_37426626delinsCTTCTT	NCBI36
NG_008135.1:g.18915_18920delinsCTTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-37_866-32delinsCTTCTT MANE Select	ENSP00000313432.6:n.866-37_866-32delinsCTTCTT
ENST00000318158.10:c.866-37_866-32delinsCTTCTT	ENSP00000313432.6:n.866-37_866-32delinsCTTCTT
ENST00000460882.5:n.893-37_893-32delinsCTTCTT
ENST00000480596.5:n.1567-37_1567-32delinsCTTCTT
ENST00000491488.5:n.571-37_571-32delinsCTTCTT
ENST00000494290.1:c.*52-257_*52-252delinsCTTCTT	ENSP00000432021.1:n.*52-257_*52-252delinsCTTCTT
ENST00000497693.1:n.4434-37_4434-32delinsCTTCTT
NM_012203.1:c.866-37_866-32delinsCTTCTT	NP_036335.1:n.866-37_866-32delinsCTTCTT
XM_005251631.1:c.545-37_545-32delinsCTTCTT	XP_005251688.1:n.545-37_545-32delinsCTTCTT
XM_011518073.1:c.464-37_464-32delinsCTTCTT	XP_011516375.1:n.464-37_464-32delinsCTTCTT
XM_017015320.2:c.946-787_946-782delinsCTTCTT	XP_016870809.1:n.946-787_946-782delinsCTTCTT
XM_017015321.2:c.866-787_866-782delinsCTTCTT	XP_016870810.1:n.866-787_866-782delinsCTTCTT
XM_017015323.2:c.544-787_544-782delinsCTTCTT	XP_016870812.1:n.544-787_544-782delinsCTTCTT
XM_024447716.1:c.1219-787_1219-782delinsCTTCTT	XP_024303484.1:n.1219-787_1219-782delinsCTTCTT
XM_024447717.1:c.1139-787_1139-782delinsCTTCTT	XP_024303485.1:n.1139-787_1139-782delinsCTTCTT
XR_002956828.1:n.1234-787_1234-782delinsCTTCTT
XR_002956829.1:n.1154-787_1154-782delinsCTTCTT
XR_002956830.1:n.2286-37_2286-32delinsCTTCTT
XR_002956831.1:n.1961-37_1961-32delinsCTTCTT
XR_002956832.1:n.1285-37_1285-32delinsCTTCTT
NM_012203.2:c.866-37_866-32delinsCTTCTT MANE Select	NP_036335.1:n.866-37_866-32delinsCTTCTT