Canonical Allele Identifier: CA373443350

Gene: GRHPR

Linked Data

• COSMIC: COSM4778355 ; COSM4778356
• MyVariant Identifiers: chr9:g.37429768A>G (hg19) ; chr9:g.37429771A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429771A>G , CM000671.2:g.37429771A>G	GRCh38
NC_000009.11:g.37429768A>G , CM000671.1:g.37429768A>G	GRCh37
NC_000009.10:g.37419768A>G	NCBI36
NG_008135.1:g.12062A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.533A>G MANE Select	ENSP00000313432.6:p.Gln178Arg
ENST00000318158.10:c.533A>G	ENSP00000313432.6:p.Gln178Arg
ENST00000377824.8:n.570A>G
ENST00000460882.5:n.560A>G
ENST00000480596.5:n.1234A>G
ENST00000491488.5:n.238A>G
ENST00000494290.1:c.104A>G	ENSP00000432021.1:p.Gln35Arg
ENST00000497693.1:n.2066A>G
ENST00000607784.1:c.533A>G	ENSP00000475569.1:p.Gln178Arg
NM_012203.1:c.533A>G	NP_036335.1:p.Gln178Arg
XM_005251631.1:c.212A>G	XP_005251688.1:p.Gln71Arg
XM_011518073.1:c.131A>G	XP_011516375.1:p.Gln44Arg
XR_929374.1:n.978A>G
XM_017015320.2:c.533A>G	XP_016870809.1:p.Gln178Arg
XM_017015321.2:c.533A>G	XP_016870810.1:p.Gln178Arg
XM_017015323.2:c.131A>G	XP_016870812.1:p.Gln44Arg
XM_024447716.1:c.806A>G	XP_024303484.1:p.Gln269Arg
XM_024447717.1:c.806A>G	XP_024303485.1:p.Gln269Arg
XR_002956828.1:n.821A>G
XR_002956829.1:n.821A>G
XR_002956830.1:n.592A>G
XR_002956831.1:n.267A>G
XR_002956832.1:n.952A>G
NM_012203.2:c.533A>G MANE Select	NP_036335.1:p.Gln178Arg