Canonical Allele Identifier: CA465004068

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429742T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429745T>G , CM000671.2:g.37429745T>G	GRCh38
NC_000009.11:g.37429742T>G , CM000671.1:g.37429742T>G	GRCh37
NC_000009.10:g.37419742T>G	NCBI36
NG_008135.1:g.12036T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.507T>G MANE Select	ENSP00000313432.6:p.Ala169=
ENST00000318158.10:c.507T>G	ENSP00000313432.6:p.Ala169=
ENST00000377824.8:n.544T>G
ENST00000460882.5:n.534T>G
ENST00000480596.5:n.1208T>G
ENST00000491488.5:n.212T>G
ENST00000494290.1:c.78T>G	ENSP00000432021.1:p.Ala26=
ENST00000497693.1:n.2040T>G
ENST00000607784.1:c.507T>G	ENSP00000475569.1:p.Ala169=
NM_012203.1:c.507T>G	NP_036335.1:p.Ala169=
XM_005251631.1:c.186T>G	XP_005251688.1:p.Ala62=
XM_011518073.1:c.105T>G	XP_011516375.1:p.Ala35=
XR_929374.1:n.952T>G
XM_017015320.2:c.507T>G	XP_016870809.1:p.Ala169=
XM_017015321.2:c.507T>G	XP_016870810.1:p.Ala169=
XM_017015323.2:c.105T>G	XP_016870812.1:p.Ala35=
XM_024447716.1:c.780T>G	XP_024303484.1:p.Ala260=
XM_024447717.1:c.780T>G	XP_024303485.1:p.Ala260=
XR_002956828.1:n.795T>G
XR_002956829.1:n.795T>G
XR_002956830.1:n.566T>G
XR_002956831.1:n.241T>G
XR_002956832.1:n.926T>G
NM_012203.2:c.507T>G MANE Select	NP_036335.1:p.Ala169=