Canonical Allele Identifier: CA373442951

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429729G>T (hg19) ; chr9:g.37429732G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429732G>T , CM000671.2:g.37429732G>T	GRCh38
NC_000009.11:g.37429729G>T , CM000671.1:g.37429729G>T	GRCh37
NC_000009.10:g.37419729G>T	NCBI36
NG_008135.1:g.12023G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.494G>T MANE Select	ENSP00000313432.6:p.Gly165Val
ENST00000318158.10:c.494G>T	ENSP00000313432.6:p.Gly165Val
ENST00000377824.8:n.531G>T
ENST00000460882.5:n.521G>T
ENST00000480596.5:n.1195G>T
ENST00000491488.5:n.199G>T
ENST00000494290.1:c.65G>T	ENSP00000432021.1:p.Gly22Val
ENST00000497693.1:n.2027G>T
ENST00000607784.1:c.494G>T	ENSP00000475569.1:p.Gly165Val
NM_012203.1:c.494G>T	NP_036335.1:p.Gly165Val
XM_005251631.1:c.173G>T	XP_005251688.1:p.Gly58Val
XM_011518073.1:c.92G>T	XP_011516375.1:p.Gly31Val
XR_929374.1:n.939G>T
XM_017015320.2:c.494G>T	XP_016870809.1:p.Gly165Val
XM_017015321.2:c.494G>T	XP_016870810.1:p.Gly165Val
XM_017015323.2:c.92G>T	XP_016870812.1:p.Gly31Val
XM_024447716.1:c.767G>T	XP_024303484.1:p.Gly256Val
XM_024447717.1:c.767G>T	XP_024303485.1:p.Gly256Val
XR_002956828.1:n.782G>T
XR_002956829.1:n.782G>T
XR_002956830.1:n.553G>T
XR_002956831.1:n.228G>T
XR_002956832.1:n.913G>T
NM_012203.2:c.494G>T MANE Select	NP_036335.1:p.Gly165Val