Canonical Allele Identifier: CA465004105

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429790C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429793C>G , CM000671.2:g.37429793C>G	GRCh38
NC_000009.11:g.37429790C>G , CM000671.1:g.37429790C>G	GRCh37
NC_000009.10:g.37419790C>G	NCBI36
NG_008135.1:g.12084C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.555C>G MANE Select	ENSP00000313432.6:p.Arg185=
ENST00000318158.10:c.555C>G	ENSP00000313432.6:p.Arg185=
ENST00000377824.8:n.592C>G
ENST00000460882.5:n.582C>G
ENST00000480596.5:n.1256C>G
ENST00000482603.1:n.8C>G
ENST00000491488.5:n.260C>G
ENST00000494290.1:c.126C>G	ENSP00000432021.1:p.Arg42=
ENST00000497693.1:n.2088C>G
ENST00000607784.1:c.555C>G	ENSP00000475569.1:p.Arg185=
NM_012203.1:c.555C>G	NP_036335.1:p.Arg185=
XM_005251631.1:c.234C>G	XP_005251688.1:p.Arg78=
XM_011518073.1:c.153C>G	XP_011516375.1:p.Arg51=
XR_929374.1:n.1000C>G
XM_017015320.2:c.555C>G	XP_016870809.1:p.Arg185=
XM_017015321.2:c.555C>G	XP_016870810.1:p.Arg185=
XM_017015323.2:c.153C>G	XP_016870812.1:p.Arg51=
XM_024447716.1:c.828C>G	XP_024303484.1:p.Arg276=
XM_024447717.1:c.828C>G	XP_024303485.1:p.Arg276=
XR_002956828.1:n.843C>G
XR_002956829.1:n.843C>G
XR_002956830.1:n.614C>G
XR_002956831.1:n.289C>G
XR_002956832.1:n.974C>G
NM_012203.2:c.555C>G MANE Select	NP_036335.1:p.Arg185=