Canonical Allele Identifier: CA465004362

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37432083G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432086G>T , CM000671.2:g.37432086G>T	GRCh38
NC_000009.11:g.37432083G>T , CM000671.1:g.37432083G>T	GRCh37
NC_000009.10:g.37422083G>T	NCBI36
NG_008135.1:g.14377G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.813G>T MANE Select	ENSP00000313432.6:p.Thr271=
ENST00000318158.10:c.813G>T	ENSP00000313432.6:p.Thr271=
ENST00000460882.5:n.840G>T
ENST00000480596.5:n.1514G>T
ENST00000482603.1:n.266G>T
ENST00000491488.5:n.518G>T
ENST00000494290.1:c.*51+935G>T	ENSP00000432021.1:n.*51+935G>T
ENST00000497693.1:n.4381G>T
ENST00000607784.1:c.813G>T	ENSP00000475569.1:p.Thr271=
NM_012203.1:c.813G>T	NP_036335.1:p.Thr271=
XM_005251631.1:c.492G>T	XP_005251688.1:p.Thr164=
XM_011518073.1:c.411G>T	XP_011516375.1:p.Thr137=
XM_017015320.2:c.813G>T	XP_016870809.1:p.Thr271=
XM_017015321.2:c.813G>T	XP_016870810.1:p.Thr271=
XM_017015323.2:c.411G>T	XP_016870812.1:p.Thr137=
XM_024447716.1:c.1086G>T	XP_024303484.1:p.Thr362=
XM_024447717.1:c.1086G>T	XP_024303485.1:p.Thr362=
XR_002956828.1:n.1101G>T
XR_002956829.1:n.1101G>T
XR_002956830.1:n.2233G>T
XR_002956831.1:n.1908G>T
XR_002956832.1:n.1232G>T
NM_012203.2:c.813G>T MANE Select	NP_036335.1:p.Thr271=