Canonical Allele Identifier: CA1846886084

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436788_37436791delinsCAGT , CM000671.2:g.37436788_37436791delinsCAGT	GRCh38
NC_000009.11:g.37436785_37436788delinsCAGT , CM000671.1:g.37436785_37436788delinsCAGT	GRCh37
NC_000009.10:g.37426785_37426788delinsCAGT	NCBI36
NG_008135.1:g.19079_19082delinsCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*6_*9delinsCAGT MANE Select	ENSP00000313432.6:n.*6_*9delinsCAGT
ENST00000318158.10:c.*6_*9delinsCAGT	ENSP00000313432.6:n.*6_*9delinsCAGT
ENST00000460882.5:n.1020_1023delinsCAGT
ENST00000480596.5:n.1694_1697delinsCAGT
ENST00000494290.1:c.*52-93_*52-90delinsCAGT	ENSP00000432021.1:n.*52-93_*52-90delinsCAGT
ENST00000497693.1:n.4561_4564delinsCAGT
NM_012203.1:c.*6_*9delinsCAGT	NP_036335.1:n.*6_*9delinsCAGT
XM_005251631.1:c.*6_*9delinsCAGT	XP_005251688.1:n.*6_*9delinsCAGT
XM_011518073.1:c.*6_*9delinsCAGT	XP_011516375.1:n.*6_*9delinsCAGT
XM_017015320.2:c.946-623_946-620delinsCAGT	XP_016870809.1:n.946-623_946-620delinsCAGT
XM_017015321.2:c.866-623_866-620delinsCAGT	XP_016870810.1:n.866-623_866-620delinsCAGT
XM_017015323.2:c.544-623_544-620delinsCAGT	XP_016870812.1:n.544-623_544-620delinsCAGT
XM_024447716.1:c.1219-623_1219-620delinsCAGT	XP_024303484.1:n.1219-623_1219-620delinsCAGT
XM_024447717.1:c.1139-623_1139-620delinsCAGT	XP_024303485.1:n.1139-623_1139-620delinsCAGT
XR_002956828.1:n.1234-623_1234-620delinsCAGT
XR_002956829.1:n.1154-623_1154-620delinsCAGT
XR_002956830.1:n.2413_2416delinsCAGT
XR_002956831.1:n.2088_2091delinsCAGT
XR_002956832.1:n.1412_1415delinsCAGT
NM_012203.2:c.*6_*9delinsCAGT MANE Select	NP_036335.1:n.*6_*9delinsCAGT