Canonical Allele Identifier: CA2783586160

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432041_37432042insCAAT , CM000671.2:g.37432041_37432042insCAAT	GRCh38
NC_000009.11:g.37432038_37432039insCAAT , CM000671.1:g.37432038_37432039insCAAT	GRCh37
NC_000009.10:g.37422038_37422039insCAAT	NCBI36
NG_008135.1:g.14332_14333insCAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.768_769insCAAT MANE Select	ENSP00000313432.6:p.Ala257GlnfsTer7
ENST00000318158.10:c.768_769insCAAT	ENSP00000313432.6:p.Ala257GlnfsTer7
ENST00000460882.5:n.795_796insCAAT
ENST00000480596.5:n.1469_1470insCAAT
ENST00000482603.1:n.221_222insCAAT
ENST00000491488.5:n.473_474insCAAT
ENST00000494290.1:c.*51+890_*51+891insCAAT	ENSP00000432021.1:n.*51+890_*51+891insCAAT
ENST00000497693.1:n.4336_4337insCAAT
ENST00000607784.1:c.768_769insCAAT	ENSP00000475569.1:p.Ala257GlnfsTer7
NM_012203.1:c.768_769insCAAT	NP_036335.1:p.Ala257GlnfsTer7
XM_005251631.1:c.447_448insCAAT	XP_005251688.1:p.Ala150GlnfsTer7
XM_011518073.1:c.366_367insCAAT	XP_011516375.1:p.Ala123GlnfsTer7
XM_017015320.2:c.768_769insCAAT	XP_016870809.1:p.Ala257GlnfsTer7
XM_017015321.2:c.768_769insCAAT	XP_016870810.1:p.Ala257GlnfsTer7
XM_017015323.2:c.366_367insCAAT	XP_016870812.1:p.Ala123GlnfsTer7
XM_024447716.1:c.1041_1042insCAAT	XP_024303484.1:p.Ala348GlnfsTer7
XM_024447717.1:c.1041_1042insCAAT	XP_024303485.1:p.Ala348GlnfsTer7
XR_002956828.1:n.1056_1057insCAAT
XR_002956829.1:n.1056_1057insCAAT
XR_002956830.1:n.2188_2189insCAAT
XR_002956831.1:n.1863_1864insCAAT
XR_002956832.1:n.1187_1188insCAAT
NM_012203.2:c.768_769insCAAT MANE Select	NP_036335.1:p.Ala257GlnfsTer7