Canonical Allele Identifier: CA373443343

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429767C>A (hg19) ; chr9:g.37429770C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429770C>A , CM000671.2:g.37429770C>A	GRCh38
NC_000009.11:g.37429767C>A , CM000671.1:g.37429767C>A	GRCh37
NC_000009.10:g.37419767C>A	NCBI36
NG_008135.1:g.12061C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.532C>A MANE Select	ENSP00000313432.6:p.Gln178Lys
ENST00000318158.10:c.532C>A	ENSP00000313432.6:p.Gln178Lys
ENST00000377824.8:n.569C>A
ENST00000460882.5:n.559C>A
ENST00000480596.5:n.1233C>A
ENST00000491488.5:n.237C>A
ENST00000494290.1:c.103C>A	ENSP00000432021.1:p.Gln35Lys
ENST00000497693.1:n.2065C>A
ENST00000607784.1:c.532C>A	ENSP00000475569.1:p.Gln178Lys
NM_012203.1:c.532C>A	NP_036335.1:p.Gln178Lys
XM_005251631.1:c.211C>A	XP_005251688.1:p.Gln71Lys
XM_011518073.1:c.130C>A	XP_011516375.1:p.Gln44Lys
XR_929374.1:n.977C>A
XM_017015320.2:c.532C>A	XP_016870809.1:p.Gln178Lys
XM_017015321.2:c.532C>A	XP_016870810.1:p.Gln178Lys
XM_017015323.2:c.130C>A	XP_016870812.1:p.Gln44Lys
XM_024447716.1:c.805C>A	XP_024303484.1:p.Gln269Lys
XM_024447717.1:c.805C>A	XP_024303485.1:p.Gln269Lys
XR_002956828.1:n.820C>A
XR_002956829.1:n.820C>A
XR_002956830.1:n.591C>A
XR_002956831.1:n.266C>A
XR_002956832.1:n.951C>A
NM_012203.2:c.532C>A MANE Select	NP_036335.1:p.Gln178Lys