Canonical Allele Identifier: CA373442754

Gene: GRHPR

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.443G>A MANE Select	ENSP00000313432.6:p.Gly148Asp
ENST00000318158.10:c.443G>A	ENSP00000313432.6:p.Gly148Asp
ENST00000377824.8:n.480G>A
ENST00000460882.5:n.470G>A
ENST00000491488.5:n.148G>A
ENST00000493368.5:n.500G>A
ENST00000497693.1:n.817G>A
ENST00000607784.1:c.443G>A	ENSP00000475569.1:p.Gly148Asp
NM_012203.1:c.443G>A	NP_036335.1:p.Gly148Asp
XM_005251631.1:c.122G>A	XP_005251688.1:p.Gly41Asp
XM_011518073.1:c.-320G>A	XP_011516375.1:n.-320G>A
XR_929374.1:n.528G>A
XM_017015320.2:c.443G>A	XP_016870809.1:p.Gly148Asp
XM_017015321.2:c.443G>A	XP_016870810.1:p.Gly148Asp
XM_017015323.2:c.-320G>A	XP_016870812.1:n.-320G>A
XM_024447716.1:c.716G>A	XP_024303484.1:p.Gly239Asp
XM_024447717.1:c.716G>A	XP_024303485.1:p.Gly239Asp
XR_002956828.1:n.731G>A
XR_002956829.1:n.731G>A
XR_002956830.1:n.502G>A
XR_002956831.1:n.177G>A
XR_002956832.1:n.502G>A
NM_012203.2:c.443G>A MANE Select	NP_036335.1:p.Gly148Asp