Canonical Allele Identifier: CA373443443

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429794C>G (hg19) ; chr9:g.37429797C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429797C>G , CM000671.2:g.37429797C>G	GRCh38
NC_000009.11:g.37429794C>G , CM000671.1:g.37429794C>G	GRCh37
NC_000009.10:g.37419794C>G	NCBI36
NG_008135.1:g.12088C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.559C>G MANE Select	ENSP00000313432.6:p.Pro187Ala
ENST00000318158.10:c.559C>G	ENSP00000313432.6:p.Pro187Ala
ENST00000377824.8:n.596C>G
ENST00000460882.5:n.586C>G
ENST00000480596.5:n.1260C>G
ENST00000482603.1:n.12C>G
ENST00000491488.5:n.264C>G
ENST00000494290.1:c.130C>G	ENSP00000432021.1:p.Pro44Ala
ENST00000497693.1:n.2092C>G
ENST00000607784.1:c.559C>G	ENSP00000475569.1:p.Pro187Ala
NM_012203.1:c.559C>G	NP_036335.1:p.Pro187Ala
XM_005251631.1:c.238C>G	XP_005251688.1:p.Pro80Ala
XM_011518073.1:c.157C>G	XP_011516375.1:p.Pro53Ala
XR_929374.1:n.1004C>G
XM_017015320.2:c.559C>G	XP_016870809.1:p.Pro187Ala
XM_017015321.2:c.559C>G	XP_016870810.1:p.Pro187Ala
XM_017015323.2:c.157C>G	XP_016870812.1:p.Pro53Ala
XM_024447716.1:c.832C>G	XP_024303484.1:p.Pro278Ala
XM_024447717.1:c.832C>G	XP_024303485.1:p.Pro278Ala
XR_002956828.1:n.847C>G
XR_002956829.1:n.847C>G
XR_002956830.1:n.618C>G
XR_002956831.1:n.293C>G
XR_002956832.1:n.978C>G
NM_012203.2:c.559C>G MANE Select	NP_036335.1:p.Pro187Ala