Canonical Allele Identifier: CA2689984637

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37436876-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436876G>A , CM000671.2:g.37436876G>A	GRCh38
NC_000009.11:g.37436873G>A , CM000671.1:g.37436873G>A	GRCh37
NC_000009.10:g.37426873G>A	NCBI36
NG_008135.1:g.19167G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*94G>A MANE Select	ENSP00000313432.6:n.*94G>A
ENST00000318158.10:c.*94G>A	ENSP00000313432.6:n.*94G>A
ENST00000480596.5:n.1782G>A
ENST00000494290.1:c.*52-5G>A	ENSP00000432021.1:n.*52-5G>A
ENST00000497693.1:n.4649G>A
NM_012203.1:c.*94G>A	NP_036335.1:n.*94G>A
XM_005251631.1:c.*94G>A	XP_005251688.1:n.*94G>A
XM_011518073.1:c.*94G>A	XP_011516375.1:n.*94G>A
XM_017015320.2:c.946-535G>A	XP_016870809.1:n.946-535G>A
XM_017015321.2:c.866-535G>A	XP_016870810.1:n.866-535G>A
XM_017015323.2:c.544-535G>A	XP_016870812.1:n.544-535G>A
XM_024447716.1:c.1219-535G>A	XP_024303484.1:n.1219-535G>A
XM_024447717.1:c.1139-535G>A	XP_024303485.1:n.1139-535G>A
XR_002956828.1:n.1234-535G>A
XR_002956829.1:n.1154-535G>A
XR_002956830.1:n.2501G>A
XR_002956831.1:n.2176G>A
XR_002956832.1:n.1500G>A
NM_012203.2:c.*94G>A MANE Select	NP_036335.1:n.*94G>A