Canonical Allele Identifier: CA465003766

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37424932C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37424935C>A , CM000671.2:g.37424935C>A	GRCh38
NC_000009.11:g.37424932C>A , CM000671.1:g.37424932C>A	GRCh37
NC_000009.10:g.37414932C>A	NCBI36
NG_008135.1:g.7226C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.174C>A MANE Select	ENSP00000313432.6:p.Leu58=
ENST00000318158.10:c.174C>A	ENSP00000313432.6:p.Leu58=
ENST00000377824.8:n.211C>A
ENST00000460882.5:n.201C>A
ENST00000487399.5:n.183C>A
ENST00000491488.5:n.109+2102C>A
ENST00000493368.5:n.231C>A
ENST00000607784.1:c.174C>A	ENSP00000475569.1:p.Leu58=
NM_012203.1:c.174C>A	NP_036335.1:p.Leu58=
XM_005251631.1:c.83+2102C>A	XP_005251688.1:n.83+2102C>A
XM_011518073.1:c.-589C>A	XP_011516375.1:n.-589C>A
XR_929374.1:n.259C>A
XM_017015320.2:c.174C>A	XP_016870809.1:p.Leu58=
XM_017015321.2:c.174C>A	XP_016870810.1:p.Leu58=
XM_017015323.2:c.-589C>A	XP_016870812.1:n.-589C>A
XM_024447716.1:c.447C>A	XP_024303484.1:p.Leu149=
XM_024447717.1:c.447C>A	XP_024303485.1:p.Leu149=
XR_002956828.1:n.462C>A
XR_002956829.1:n.462C>A
XR_002956830.1:n.233C>A
XR_002956831.1:n.138+2102C>A
XR_002956832.1:n.233C>A
NM_012203.2:c.174C>A MANE Select	NP_036335.1:p.Leu58=