Canonical Allele Identifier: CA373442421

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37426540T>G (hg19) ; chr9:g.37426543T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37426543T>G , CM000671.2:g.37426543T>G	GRCh38
NC_000009.11:g.37426540T>G , CM000671.1:g.37426540T>G	GRCh37
NC_000009.10:g.37416540T>G	NCBI36
NG_008135.1:g.8834T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.293T>G MANE Select	ENSP00000313432.6:p.Ile98Ser
ENST00000318158.10:c.293T>G	ENSP00000313432.6:p.Ile98Ser
ENST00000377824.8:n.330T>G
ENST00000460882.5:n.320T>G
ENST00000487399.5:n.845T>G
ENST00000491488.5:n.110-1941T>G
ENST00000493368.5:n.350T>G
ENST00000607784.1:c.293T>G	ENSP00000475569.1:p.Ile98Ser
NM_012203.1:c.293T>G	NP_036335.1:p.Ile98Ser
XM_005251631.1:c.84-1941T>G	XP_005251688.1:n.84-1941T>G
XM_011518073.1:c.-470T>G	XP_011516375.1:n.-470T>G
XR_929374.1:n.378T>G
XM_017015320.2:c.293T>G	XP_016870809.1:p.Ile98Ser
XM_017015321.2:c.293T>G	XP_016870810.1:p.Ile98Ser
XM_017015323.2:c.-470T>G	XP_016870812.1:n.-470T>G
XM_024447716.1:c.566T>G	XP_024303484.1:p.Ile189Ser
XM_024447717.1:c.566T>G	XP_024303485.1:p.Ile189Ser
XR_002956828.1:n.581T>G
XR_002956829.1:n.581T>G
XR_002956830.1:n.352T>G
XR_002956831.1:n.139-1941T>G
XR_002956832.1:n.352T>G
NM_012203.2:c.293T>G MANE Select	NP_036335.1:p.Ile98Ser