Canonical Allele Identifier: CA373443420

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429786G>T (hg19) ; chr9:g.37429789G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429789G>T , CM000671.2:g.37429789G>T	GRCh38
NC_000009.11:g.37429786G>T , CM000671.1:g.37429786G>T	GRCh37
NC_000009.10:g.37419786G>T	NCBI36
NG_008135.1:g.12080G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.551G>T MANE Select	ENSP00000313432.6:p.Gly184Val
ENST00000318158.10:c.551G>T	ENSP00000313432.6:p.Gly184Val
ENST00000377824.8:n.588G>T
ENST00000460882.5:n.578G>T
ENST00000480596.5:n.1252G>T
ENST00000482603.1:n.4G>T
ENST00000491488.5:n.256G>T
ENST00000494290.1:c.122G>T	ENSP00000432021.1:p.Gly41Val
ENST00000497693.1:n.2084G>T
ENST00000607784.1:c.551G>T	ENSP00000475569.1:p.Gly184Val
NM_012203.1:c.551G>T	NP_036335.1:p.Gly184Val
XM_005251631.1:c.230G>T	XP_005251688.1:p.Gly77Val
XM_011518073.1:c.149G>T	XP_011516375.1:p.Gly50Val
XR_929374.1:n.996G>T
XM_017015320.2:c.551G>T	XP_016870809.1:p.Gly184Val
XM_017015321.2:c.551G>T	XP_016870810.1:p.Gly184Val
XM_017015323.2:c.149G>T	XP_016870812.1:p.Gly50Val
XM_024447716.1:c.824G>T	XP_024303484.1:p.Gly275Val
XM_024447717.1:c.824G>T	XP_024303485.1:p.Gly275Val
XR_002956828.1:n.839G>T
XR_002956829.1:n.839G>T
XR_002956830.1:n.610G>T
XR_002956831.1:n.285G>T
XR_002956832.1:n.970G>T
NM_012203.2:c.551G>T MANE Select	NP_036335.1:p.Gly184Val