Canonical Allele Identifier: CA465004123

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429823G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429826G>A , CM000671.2:g.37429826G>A	GRCh38
NC_000009.11:g.37429823G>A , CM000671.1:g.37429823G>A	GRCh37
NC_000009.10:g.37419823G>A	NCBI36
NG_008135.1:g.12117G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.588G>A MANE Select	ENSP00000313432.6:p.Gln196=
ENST00000318158.10:c.588G>A	ENSP00000313432.6:p.Gln196=
ENST00000377824.8:n.625G>A
ENST00000460882.5:n.615G>A
ENST00000480596.5:n.1289G>A
ENST00000482603.1:n.41G>A
ENST00000491488.5:n.293G>A
ENST00000494290.1:c.159G>A	ENSP00000432021.1:p.Gln53=
ENST00000497693.1:n.2121G>A
ENST00000607784.1:c.588G>A	ENSP00000475569.1:p.Gln196=
NM_012203.1:c.588G>A	NP_036335.1:p.Gln196=
XM_005251631.1:c.267G>A	XP_005251688.1:p.Gln89=
XM_011518073.1:c.186G>A	XP_011516375.1:p.Gln62=
XR_929374.1:n.1033G>A
XM_017015320.2:c.588G>A	XP_016870809.1:p.Gln196=
XM_017015321.2:c.588G>A	XP_016870810.1:p.Gln196=
XM_017015323.2:c.186G>A	XP_016870812.1:p.Gln62=
XM_024447716.1:c.861G>A	XP_024303484.1:p.Gln287=
XM_024447717.1:c.861G>A	XP_024303485.1:p.Gln287=
XR_002956828.1:n.876G>A
XR_002956829.1:n.876G>A
XR_002956830.1:n.647G>A
XR_002956831.1:n.322G>A
XR_002956832.1:n.1007G>A
NM_012203.2:c.588G>A MANE Select	NP_036335.1:p.Gln196=