Canonical Allele Identifier: CA2689954133

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37428328-TCTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428330_37428332del , CM000671.2:g.37428330_37428332del	GRCh38
NC_000009.11:g.37428327_37428329del , CM000671.1:g.37428327_37428329del	GRCh37
NC_000009.10:g.37418327_37418329del	NCBI36
NG_008135.1:g.10621_10623del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.405-154_405-152del MANE Select	ENSP00000313432.6:n.405-154_405-152del
ENST00000318158.10:c.405-154_405-152del	ENSP00000313432.6:n.405-154_405-152del
ENST00000377824.8:n.442-154_442-152del
ENST00000460882.5:n.432-154_432-152del
ENST00000491488.5:n.110-154_110-152del
ENST00000493368.5:n.462-154_462-152del
ENST00000497693.1:n.625_627del
ENST00000607784.1:c.405-154_405-152del	ENSP00000475569.1:n.405-154_405-152del
NM_012203.1:c.405-154_405-152del	NP_036335.1:n.405-154_405-152del
XM_005251631.1:c.84-154_84-152del	XP_005251688.1:n.84-154_84-152del
XM_011518073.1:c.-358-154_-358-152del	XP_011516375.1:n.-358-154_-358-152del
XR_929374.1:n.490-154_490-152del
XM_017015320.2:c.405-154_405-152del	XP_016870809.1:n.405-154_405-152del
XM_017015321.2:c.405-154_405-152del	XP_016870810.1:n.405-154_405-152del
XM_017015323.2:c.-358-154_-358-152del	XP_016870812.1:n.-358-154_-358-152del
XM_024447716.1:c.678-154_678-152del	XP_024303484.1:n.678-154_678-152del
XM_024447717.1:c.678-154_678-152del	XP_024303485.1:n.678-154_678-152del
XR_002956828.1:n.693-154_693-152del
XR_002956829.1:n.693-154_693-152del
XR_002956830.1:n.464-154_464-152del
XR_002956831.1:n.139-154_139-152del
XR_002956832.1:n.464-154_464-152del
NM_012203.2:c.405-154_405-152del MANE Select	NP_036335.1:n.405-154_405-152del