Canonical Allele Identifier: CA2689984685

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436933-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436933T>A , CM000671.2:g.37436933T>A	GRCh38
NC_000009.11:g.37436930T>A , CM000671.1:g.37436930T>A	GRCh37
NC_000009.10:g.37426930T>A	NCBI36
NG_008135.1:g.19224T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*151T>A MANE Select	ENSP00000313432.6:n.*151T>A
ENST00000318158.10:c.*151T>A	ENSP00000313432.6:n.*151T>A
ENST00000480596.5:n.1839T>A
ENST00000494290.1:c.*104T>A	ENSP00000432021.1:n.*104T>A
ENST00000497693.1:n.4706T>A
NM_012203.1:c.*151T>A	NP_036335.1:n.*151T>A
XM_005251631.1:c.*151T>A	XP_005251688.1:n.*151T>A
XM_011518073.1:c.*151T>A	XP_011516375.1:n.*151T>A
XM_017015320.2:c.946-478T>A	XP_016870809.1:n.946-478T>A
XM_017015321.2:c.866-478T>A	XP_016870810.1:n.866-478T>A
XM_017015323.2:c.544-478T>A	XP_016870812.1:n.544-478T>A
XM_024447716.1:c.1219-478T>A	XP_024303484.1:n.1219-478T>A
XM_024447717.1:c.1139-478T>A	XP_024303485.1:n.1139-478T>A
XR_002956828.1:n.1234-478T>A
XR_002956829.1:n.1154-478T>A
XR_002956830.1:n.2558T>A
XR_002956831.1:n.2233T>A
XR_002956832.1:n.1557T>A
NM_012203.2:c.*151T>A MANE Select	NP_036335.1:n.*151T>A