Canonical Allele Identifier: CA2689954155

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37428335-TGCCGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428337_37428341del , CM000671.2:g.37428337_37428341del	GRCh38
NC_000009.11:g.37428334_37428338del , CM000671.1:g.37428334_37428338del	GRCh37
NC_000009.10:g.37418334_37418338del	NCBI36
NG_008135.1:g.10628_10632del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.405-147_405-143del MANE Select	ENSP00000313432.6:n.405-147_405-143del
ENST00000318158.10:c.405-147_405-143del	ENSP00000313432.6:n.405-147_405-143del
ENST00000377824.8:n.442-147_442-143del
ENST00000460882.5:n.432-147_432-143del
ENST00000491488.5:n.110-147_110-143del
ENST00000493368.5:n.462-147_462-143del
ENST00000497693.1:n.632_636del
ENST00000607784.1:c.405-147_405-143del	ENSP00000475569.1:n.405-147_405-143del
NM_012203.1:c.405-147_405-143del	NP_036335.1:n.405-147_405-143del
XM_005251631.1:c.84-147_84-143del	XP_005251688.1:n.84-147_84-143del
XM_011518073.1:c.-358-147_-358-143del	XP_011516375.1:n.-358-147_-358-143del
XR_929374.1:n.490-147_490-143del
XM_017015320.2:c.405-147_405-143del	XP_016870809.1:n.405-147_405-143del
XM_017015321.2:c.405-147_405-143del	XP_016870810.1:n.405-147_405-143del
XM_017015323.2:c.-358-147_-358-143del	XP_016870812.1:n.-358-147_-358-143del
XM_024447716.1:c.678-147_678-143del	XP_024303484.1:n.678-147_678-143del
XM_024447717.1:c.678-147_678-143del	XP_024303485.1:n.678-147_678-143del
XR_002956828.1:n.693-147_693-143del
XR_002956829.1:n.693-147_693-143del
XR_002956830.1:n.464-147_464-143del
XR_002956831.1:n.139-147_139-143del
XR_002956832.1:n.464-147_464-143del
NM_012203.2:c.405-147_405-143del MANE Select	NP_036335.1:n.405-147_405-143del