Canonical Allele Identifier: CA465004365

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37432092-A-G
• MyVariant Identifiers: chr9:g.37432089A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432092A>G , CM000671.2:g.37432092A>G	GRCh38
NC_000009.11:g.37432089A>G , CM000671.1:g.37432089A>G	GRCh37
NC_000009.10:g.37422089A>G	NCBI36
NG_008135.1:g.14383A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.819A>G MANE Select	ENSP00000313432.6:p.Pro273=
ENST00000318158.10:c.819A>G	ENSP00000313432.6:p.Pro273=
ENST00000460882.5:n.846A>G
ENST00000480596.5:n.1520A>G
ENST00000482603.1:n.272A>G
ENST00000491488.5:n.524A>G
ENST00000494290.1:c.*51+941A>G	ENSP00000432021.1:n.*51+941A>G
ENST00000497693.1:n.4387A>G
ENST00000512404.2:n.6A>G
ENST00000607784.1:c.819A>G	ENSP00000475569.1:p.Pro273=
NM_012203.1:c.819A>G	NP_036335.1:p.Pro273=
XM_005251631.1:c.498A>G	XP_005251688.1:p.Pro166=
XM_011518073.1:c.417A>G	XP_011516375.1:p.Pro139=
XM_017015320.2:c.819A>G	XP_016870809.1:p.Pro273=
XM_017015321.2:c.819A>G	XP_016870810.1:p.Pro273=
XM_017015323.2:c.417A>G	XP_016870812.1:p.Pro139=
XM_024447716.1:c.1092A>G	XP_024303484.1:p.Pro364=
XM_024447717.1:c.1092A>G	XP_024303485.1:p.Pro364=
XR_002956828.1:n.1107A>G
XR_002956829.1:n.1107A>G
XR_002956830.1:n.2239A>G
XR_002956831.1:n.1914A>G
XR_002956832.1:n.1238A>G
NM_012203.2:c.819A>G MANE Select	NP_036335.1:p.Pro273=