Canonical Allele Identifier: CA373442731

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37428509T>A (hg19) ; chr9:g.37428512T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428512T>A , CM000671.2:g.37428512T>A	GRCh38
NC_000009.11:g.37428509T>A , CM000671.1:g.37428509T>A	GRCh37
NC_000009.10:g.37418509T>A	NCBI36
NG_008135.1:g.10803T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.433T>A MANE Select	ENSP00000313432.6:p.Trp145Arg
ENST00000318158.10:c.433T>A	ENSP00000313432.6:p.Trp145Arg
ENST00000377824.8:n.470T>A
ENST00000460882.5:n.460T>A
ENST00000491488.5:n.138T>A
ENST00000493368.5:n.490T>A
ENST00000497693.1:n.807T>A
ENST00000607784.1:c.433T>A	ENSP00000475569.1:p.Trp145Arg
NM_012203.1:c.433T>A	NP_036335.1:p.Trp145Arg
XM_005251631.1:c.112T>A	XP_005251688.1:p.Trp38Arg
XM_011518073.1:c.-330T>A	XP_011516375.1:n.-330T>A
XR_929374.1:n.518T>A
XM_017015320.2:c.433T>A	XP_016870809.1:p.Trp145Arg
XM_017015321.2:c.433T>A	XP_016870810.1:p.Trp145Arg
XM_017015323.2:c.-330T>A	XP_016870812.1:n.-330T>A
XM_024447716.1:c.706T>A	XP_024303484.1:p.Trp236Arg
XM_024447717.1:c.706T>A	XP_024303485.1:p.Trp236Arg
XR_002956828.1:n.721T>A
XR_002956829.1:n.721T>A
XR_002956830.1:n.492T>A
XR_002956831.1:n.167T>A
XR_002956832.1:n.492T>A
NM_012203.2:c.433T>A MANE Select	NP_036335.1:p.Trp145Arg