Canonical Allele Identifier: CA465004377

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37432101T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432104T>G , CM000671.2:g.37432104T>G	GRCh38
NC_000009.11:g.37432101T>G , CM000671.1:g.37432101T>G	GRCh37
NC_000009.10:g.37422101T>G	NCBI36
NG_008135.1:g.14395T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.831T>G MANE Select	ENSP00000313432.6:p.Pro277=
ENST00000318158.10:c.831T>G	ENSP00000313432.6:p.Pro277=
ENST00000460882.5:n.858T>G
ENST00000480596.5:n.1532T>G
ENST00000482603.1:n.284T>G
ENST00000491488.5:n.536T>G
ENST00000494290.1:c.*51+953T>G	ENSP00000432021.1:n.*51+953T>G
ENST00000497693.1:n.4399T>G
ENST00000512404.2:n.18T>G
ENST00000607784.1:c.831T>G	ENSP00000475569.1:p.Pro277=
NM_012203.1:c.831T>G	NP_036335.1:p.Pro277=
XM_005251631.1:c.510T>G	XP_005251688.1:p.Pro170=
XM_011518073.1:c.429T>G	XP_011516375.1:p.Pro143=
XM_017015320.2:c.831T>G	XP_016870809.1:p.Pro277=
XM_017015321.2:c.831T>G	XP_016870810.1:p.Pro277=
XM_017015323.2:c.429T>G	XP_016870812.1:p.Pro143=
XM_024447716.1:c.1104T>G	XP_024303484.1:p.Pro368=
XM_024447717.1:c.1104T>G	XP_024303485.1:p.Pro368=
XR_002956828.1:n.1119T>G
XR_002956829.1:n.1119T>G
XR_002956830.1:n.2251T>G
XR_002956831.1:n.1926T>G
XR_002956832.1:n.1250T>G
NM_012203.2:c.831T>G MANE Select	NP_036335.1:p.Pro277=