Canonical Allele Identifier: CA465006805

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37436668C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436671C>G , CM000671.2:g.37436671C>G	GRCh38
NC_000009.11:g.37436668C>G , CM000671.1:g.37436668C>G	GRCh37
NC_000009.10:g.37426668C>G	NCBI36
NG_008135.1:g.18962C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.876C>G MANE Select	ENSP00000313432.6:p.Pro292=
ENST00000318158.10:c.876C>G	ENSP00000313432.6:p.Pro292=
ENST00000460882.5:n.903C>G
ENST00000480596.5:n.1577C>G
ENST00000491488.5:n.581C>G
ENST00000494290.1:c.*52-210C>G	ENSP00000432021.1:n.*52-210C>G
ENST00000497693.1:n.4444C>G
NM_012203.1:c.876C>G	NP_036335.1:p.Pro292=
XM_005251631.1:c.555C>G	XP_005251688.1:p.Pro185=
XM_011518073.1:c.474C>G	XP_011516375.1:p.Pro158=
XM_017015320.2:c.946-740C>G	XP_016870809.1:n.946-740C>G
XM_017015321.2:c.866-740C>G	XP_016870810.1:n.866-740C>G
XM_017015323.2:c.544-740C>G	XP_016870812.1:n.544-740C>G
XM_024447716.1:c.1219-740C>G	XP_024303484.1:n.1219-740C>G
XM_024447717.1:c.1139-740C>G	XP_024303485.1:n.1139-740C>G
XR_002956828.1:n.1234-740C>G
XR_002956829.1:n.1154-740C>G
XR_002956830.1:n.2296C>G
XR_002956831.1:n.1971C>G
XR_002956832.1:n.1295C>G
NM_012203.2:c.876C>G MANE Select	NP_036335.1:p.Pro292=