Canonical Allele Identifier: CA1846868922

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428467_37428469delinsCCT , CM000671.2:g.37428467_37428469delinsCCT	GRCh38
NC_000009.11:g.37428464_37428466delinsCCT , CM000671.1:g.37428464_37428466delinsCCT	GRCh37
NC_000009.10:g.37418464_37418466delinsCCT	NCBI36
NG_008135.1:g.10758_10760delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.405-17_405-15delinsCCT MANE Select	ENSP00000313432.6:n.405-17_405-15delinsCCT
ENST00000318158.10:c.405-17_405-15delinsCCT	ENSP00000313432.6:n.405-17_405-15delinsCCT
ENST00000377824.8:n.442-17_442-15delinsCCT
ENST00000460882.5:n.432-17_432-15delinsCCT
ENST00000491488.5:n.110-17_110-15delinsCCT
ENST00000493368.5:n.462-17_462-15delinsCCT
ENST00000497693.1:n.762_764delinsCCT
ENST00000607784.1:c.405-17_405-15delinsCCT	ENSP00000475569.1:n.405-17_405-15delinsCCT
NM_012203.1:c.405-17_405-15delinsCCT	NP_036335.1:n.405-17_405-15delinsCCT
XM_005251631.1:c.84-17_84-15delinsCCT	XP_005251688.1:n.84-17_84-15delinsCCT
XM_011518073.1:c.-358-17_-358-15delinsCCT	XP_011516375.1:n.-358-17_-358-15delinsCCT
XR_929374.1:n.490-17_490-15delinsCCT
XM_017015320.2:c.405-17_405-15delinsCCT	XP_016870809.1:n.405-17_405-15delinsCCT
XM_017015321.2:c.405-17_405-15delinsCCT	XP_016870810.1:n.405-17_405-15delinsCCT
XM_017015323.2:c.-358-17_-358-15delinsCCT	XP_016870812.1:n.-358-17_-358-15delinsCCT
XM_024447716.1:c.678-17_678-15delinsCCT	XP_024303484.1:n.678-17_678-15delinsCCT
XM_024447717.1:c.678-17_678-15delinsCCT	XP_024303485.1:n.678-17_678-15delinsCCT
XR_002956828.1:n.693-17_693-15delinsCCT
XR_002956829.1:n.693-17_693-15delinsCCT
XR_002956830.1:n.464-17_464-15delinsCCT
XR_002956831.1:n.139-17_139-15delinsCCT
XR_002956832.1:n.464-17_464-15delinsCCT
NM_012203.2:c.405-17_405-15delinsCCT MANE Select	NP_036335.1:n.405-17_405-15delinsCCT