Canonical Allele Identifier: CA465006855

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37436737T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436740T>G , CM000671.2:g.37436740T>G	GRCh38
NC_000009.11:g.37436737T>G , CM000671.1:g.37436737T>G	GRCh37
NC_000009.10:g.37426737T>G	NCBI36
NG_008135.1:g.19031T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.945T>G MANE Select	ENSP00000313432.6:p.Ala315=
ENST00000318158.10:c.945T>G	ENSP00000313432.6:p.Ala315=
ENST00000460882.5:n.972T>G
ENST00000480596.5:n.1646T>G
ENST00000494290.1:c.*52-141T>G	ENSP00000432021.1:n.*52-141T>G
ENST00000497693.1:n.4513T>G
NM_012203.1:c.945T>G	NP_036335.1:p.Ala315=
XM_005251631.1:c.624T>G	XP_005251688.1:p.Ala208=
XM_011518073.1:c.543T>G	XP_011516375.1:p.Ala181=
XM_017015320.2:c.946-671T>G	XP_016870809.1:n.946-671T>G
XM_017015321.2:c.866-671T>G	XP_016870810.1:n.866-671T>G
XM_017015323.2:c.544-671T>G	XP_016870812.1:n.544-671T>G
XM_024447716.1:c.1219-671T>G	XP_024303484.1:n.1219-671T>G
XM_024447717.1:c.1139-671T>G	XP_024303485.1:n.1139-671T>G
XR_002956828.1:n.1234-671T>G
XR_002956829.1:n.1154-671T>G
XR_002956830.1:n.2365T>G
XR_002956831.1:n.2040T>G
XR_002956832.1:n.1364T>G
NM_012203.2:c.945T>G MANE Select	NP_036335.1:p.Ala315=