Canonical Allele Identifier: CA373442755

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37428519G>C (hg19) ; chr9:g.37428522G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428522G>C , CM000671.2:g.37428522G>C	GRCh38
NC_000009.11:g.37428519G>C , CM000671.1:g.37428519G>C	GRCh37
NC_000009.10:g.37418519G>C	NCBI36
NG_008135.1:g.10813G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.443G>C MANE Select	ENSP00000313432.6:p.Gly148Ala
ENST00000318158.10:c.443G>C	ENSP00000313432.6:p.Gly148Ala
ENST00000377824.8:n.480G>C
ENST00000460882.5:n.470G>C
ENST00000491488.5:n.148G>C
ENST00000493368.5:n.500G>C
ENST00000497693.1:n.817G>C
ENST00000607784.1:c.443G>C	ENSP00000475569.1:p.Gly148Ala
NM_012203.1:c.443G>C	NP_036335.1:p.Gly148Ala
XM_005251631.1:c.122G>C	XP_005251688.1:p.Gly41Ala
XM_011518073.1:c.-320G>C	XP_011516375.1:n.-320G>C
XR_929374.1:n.528G>C
XM_017015320.2:c.443G>C	XP_016870809.1:p.Gly148Ala
XM_017015321.2:c.443G>C	XP_016870810.1:p.Gly148Ala
XM_017015323.2:c.-320G>C	XP_016870812.1:n.-320G>C
XM_024447716.1:c.716G>C	XP_024303484.1:p.Gly239Ala
XM_024447717.1:c.716G>C	XP_024303485.1:p.Gly239Ala
XR_002956828.1:n.731G>C
XR_002956829.1:n.731G>C
XR_002956830.1:n.502G>C
XR_002956831.1:n.177G>C
XR_002956832.1:n.502G>C
NM_012203.2:c.443G>C MANE Select	NP_036335.1:p.Gly148Ala