Canonical Allele Identifier: CA373442798

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37428543-C-G
• MyVariant Identifiers: chr9:g.37428540C>G (hg19) ; chr9:g.37428543C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428543C>G , CM000671.2:g.37428543C>G	GRCh38
NC_000009.11:g.37428540C>G , CM000671.1:g.37428540C>G	GRCh37
NC_000009.10:g.37418540C>G	NCBI36
NG_008135.1:g.10834C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.464C>G MANE Select	ENSP00000313432.6:p.Thr155Ser
ENST00000318158.10:c.464C>G	ENSP00000313432.6:p.Thr155Ser
ENST00000377824.8:n.501C>G
ENST00000460882.5:n.491C>G
ENST00000480596.5:n.6C>G
ENST00000491488.5:n.169C>G
ENST00000493368.5:n.521C>G
ENST00000497693.1:n.838C>G
ENST00000607784.1:c.464C>G	ENSP00000475569.1:p.Thr155Ser
NM_012203.1:c.464C>G	NP_036335.1:p.Thr155Ser
XM_005251631.1:c.143C>G	XP_005251688.1:p.Thr48Ser
XM_011518073.1:c.-299C>G	XP_011516375.1:n.-299C>G
XR_929374.1:n.549C>G
XM_017015320.2:c.464C>G	XP_016870809.1:p.Thr155Ser
XM_017015321.2:c.464C>G	XP_016870810.1:p.Thr155Ser
XM_017015323.2:c.-299C>G	XP_016870812.1:n.-299C>G
XM_024447716.1:c.737C>G	XP_024303484.1:p.Thr246Ser
XM_024447717.1:c.737C>G	XP_024303485.1:p.Thr246Ser
XR_002956828.1:n.752C>G
XR_002956829.1:n.752C>G
XR_002956830.1:n.523C>G
XR_002956831.1:n.198C>G
XR_002956832.1:n.523C>G
NM_012203.2:c.464C>G MANE Select	NP_036335.1:p.Thr155Ser