Canonical Allele Identifier: CA1846885276

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436623_37436626delinsCCTT , CM000671.2:g.37436623_37436626delinsCCTT	GRCh38
NC_000009.11:g.37436620_37436623delinsCCTT , CM000671.1:g.37436620_37436623delinsCCTT	GRCh37
NC_000009.10:g.37426620_37426623delinsCCTT	NCBI36
NG_008135.1:g.18914_18917delinsCCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.866-38_866-35delinsCCTT MANE Select	ENSP00000313432.6:n.866-38_866-35delinsCC...
ENST00000318158.10:c.866-38_866-35delinsCCTT	ENSP00000313432.6:n.866-38_866-35delinsCC...
ENST00000460882.5:n.893-38_893-35delinsCCTT
ENST00000480596.5:n.1567-38_1567-35delinsCCTT
ENST00000491488.5:n.571-38_571-35delinsCCTT
ENST00000494290.1:c.*52-258_*52-255delinsCCTT	ENSP00000432021.1:n.*52-258_*52-255delins...
ENST00000497693.1:n.4434-38_4434-35delinsCCTT
NM_012203.1:c.866-38_866-35delinsCCTT	NP_036335.1:n.866-38_866-35delinsCCTT
XM_005251631.1:c.545-38_545-35delinsCCTT	XP_005251688.1:n.545-38_545-35delinsCCTT
XM_011518073.1:c.464-38_464-35delinsCCTT	XP_011516375.1:n.464-38_464-35delinsCCTT
XM_017015320.2:c.946-788_946-785delinsCCTT	XP_016870809.1:n.946-788_946-785delinsCCT...
XM_017015321.2:c.866-788_866-785delinsCCTT	XP_016870810.1:n.866-788_866-785delinsCCT...
XM_017015323.2:c.544-788_544-785delinsCCTT	XP_016870812.1:n.544-788_544-785delinsCCT...
XM_024447716.1:c.1219-788_1219-785delinsCCTT	XP_024303484.1:n.1219-788_1219-785delinsC...
XM_024447717.1:c.1139-788_1139-785delinsCCTT	XP_024303485.1:n.1139-788_1139-785delinsC...
XR_002956828.1:n.1234-788_1234-785delinsCCTT
XR_002956829.1:n.1154-788_1154-785delinsCCTT
XR_002956830.1:n.2286-38_2286-35delinsCCTT
XR_002956831.1:n.1961-38_1961-35delinsCCTT
XR_002956832.1:n.1285-38_1285-35delinsCCTT
NM_012203.2:c.866-38_866-35delinsCCTT MANE Select	NP_036335.1:n.866-38_866-35delinsCCTT