Canonical Allele Identifier: CA373443476

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429804A>C (hg19) ; chr9:g.37429807A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429807A>C , CM000671.2:g.37429807A>C	GRCh38
NC_000009.11:g.37429804A>C , CM000671.1:g.37429804A>C	GRCh37
NC_000009.10:g.37419804A>C	NCBI36
NG_008135.1:g.12098A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.569A>C MANE Select	ENSP00000313432.6:p.Glu190Ala
ENST00000318158.10:c.569A>C	ENSP00000313432.6:p.Glu190Ala
ENST00000377824.8:n.606A>C
ENST00000460882.5:n.596A>C
ENST00000480596.5:n.1270A>C
ENST00000482603.1:n.22A>C
ENST00000491488.5:n.274A>C
ENST00000494290.1:c.140A>C	ENSP00000432021.1:p.Glu47Ala
ENST00000497693.1:n.2102A>C
ENST00000607784.1:c.569A>C	ENSP00000475569.1:p.Glu190Ala
NM_012203.1:c.569A>C	NP_036335.1:p.Glu190Ala
XM_005251631.1:c.248A>C	XP_005251688.1:p.Glu83Ala
XM_011518073.1:c.167A>C	XP_011516375.1:p.Glu56Ala
XR_929374.1:n.1014A>C
XM_017015320.2:c.569A>C	XP_016870809.1:p.Glu190Ala
XM_017015321.2:c.569A>C	XP_016870810.1:p.Glu190Ala
XM_017015323.2:c.167A>C	XP_016870812.1:p.Glu56Ala
XM_024447716.1:c.842A>C	XP_024303484.1:p.Glu281Ala
XM_024447717.1:c.842A>C	XP_024303485.1:p.Glu281Ala
XR_002956828.1:n.857A>C
XR_002956829.1:n.857A>C
XR_002956830.1:n.628A>C
XR_002956831.1:n.303A>C
XR_002956832.1:n.988A>C
NM_012203.2:c.569A>C MANE Select	NP_036335.1:p.Glu190Ala