Canonical Allele Identifier: CA465004122

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429820C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429823C>T , CM000671.2:g.37429823C>T	GRCh38
NC_000009.11:g.37429820C>T , CM000671.1:g.37429820C>T	GRCh37
NC_000009.10:g.37419820C>T	NCBI36
NG_008135.1:g.12114C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.585C>T MANE Select	ENSP00000313432.6:p.Phe195=
ENST00000318158.10:c.585C>T	ENSP00000313432.6:p.Phe195=
ENST00000377824.8:n.622C>T
ENST00000460882.5:n.612C>T
ENST00000480596.5:n.1286C>T
ENST00000482603.1:n.38C>T
ENST00000491488.5:n.290C>T
ENST00000494290.1:c.156C>T	ENSP00000432021.1:p.Phe52=
ENST00000497693.1:n.2118C>T
ENST00000607784.1:c.585C>T	ENSP00000475569.1:p.Phe195=
NM_012203.1:c.585C>T	NP_036335.1:p.Phe195=
XM_005251631.1:c.264C>T	XP_005251688.1:p.Phe88=
XM_011518073.1:c.183C>T	XP_011516375.1:p.Phe61=
XR_929374.1:n.1030C>T
XM_017015320.2:c.585C>T	XP_016870809.1:p.Phe195=
XM_017015321.2:c.585C>T	XP_016870810.1:p.Phe195=
XM_017015323.2:c.183C>T	XP_016870812.1:p.Phe61=
XM_024447716.1:c.858C>T	XP_024303484.1:p.Phe286=
XM_024447717.1:c.858C>T	XP_024303485.1:p.Phe286=
XR_002956828.1:n.873C>T
XR_002956829.1:n.873C>T
XR_002956830.1:n.644C>T
XR_002956831.1:n.319C>T
XR_002956832.1:n.1004C>T
NM_012203.2:c.585C>T MANE Select	NP_036335.1:p.Phe195=