Canonical Allele Identifier: CA1846886205

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436820_37436821delinsGC , CM000671.2:g.37436820_37436821delinsGC	GRCh38
NC_000009.11:g.37436817_37436818delinsGC , CM000671.1:g.37436817_37436818delinsGC	GRCh37
NC_000009.10:g.37426817_37426818delinsGC	NCBI36
NG_008135.1:g.19111_19112delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*38_*39delinsGC MANE Select	ENSP00000313432.6:n.*38_*39delinsGC
ENST00000318158.10:c.*38_*39delinsGC	ENSP00000313432.6:n.*38_*39delinsGC
ENST00000460882.5:n.1052_1053delinsGC
ENST00000480596.5:n.1726_1727delinsGC
ENST00000494290.1:c.*52-61_*52-60delinsGC	ENSP00000432021.1:n.*52-61_*52-60delinsGC
ENST00000497693.1:n.4593_4594delinsGC
NM_012203.1:c.*38_*39delinsGC	NP_036335.1:n.*38_*39delinsGC
XM_005251631.1:c.*38_*39delinsGC	XP_005251688.1:n.*38_*39delinsGC
XM_011518073.1:c.*38_*39delinsGC	XP_011516375.1:n.*38_*39delinsGC
XM_017015320.2:c.946-591_946-590delinsGC	XP_016870809.1:n.946-591_946-590delinsGC
XM_017015321.2:c.866-591_866-590delinsGC	XP_016870810.1:n.866-591_866-590delinsGC
XM_017015323.2:c.544-591_544-590delinsGC	XP_016870812.1:n.544-591_544-590delinsGC
XM_024447716.1:c.1219-591_1219-590delinsGC	XP_024303484.1:n.1219-591_1219-590delinsGC
XM_024447717.1:c.1139-591_1139-590delinsGC	XP_024303485.1:n.1139-591_1139-590delinsGC
XR_002956828.1:n.1234-591_1234-590delinsGC
XR_002956829.1:n.1154-591_1154-590delinsGC
XR_002956830.1:n.2445_2446delinsGC
XR_002956831.1:n.2120_2121delinsGC
XR_002956832.1:n.1444_1445delinsGC
NM_012203.2:c.*38_*39delinsGC MANE Select	NP_036335.1:n.*38_*39delinsGC