Canonical Allele Identifier: CA1846870541

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429787A= , CM000671.2:g.37429787A=	GRCh38
NC_000009.11:g.37429784A= , CM000671.1:g.37429784A=	GRCh37
NC_000009.10:g.37419784A=	NCBI36
NG_008135.1:g.12078A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.549A= MANE Select	ENSP00000313432.6:p.Thr183=
ENST00000318158.10:c.549A=	ENSP00000313432.6:p.Thr183=
ENST00000377824.8:n.586A=
ENST00000460882.5:n.576A=
ENST00000480596.5:n.1250A=
ENST00000482603.1:n.2A=
ENST00000491488.5:n.254A=
ENST00000494290.1:c.120A=	ENSP00000432021.1:p.Thr40=
ENST00000497693.1:n.2082A=
ENST00000607784.1:c.549A=	ENSP00000475569.1:p.Thr183=
NM_012203.1:c.549A=	NP_036335.1:p.Thr183=
XM_005251631.1:c.228A=	XP_005251688.1:p.Thr76=
XM_011518073.1:c.147A=	XP_011516375.1:p.Thr49=
XR_929374.1:n.994A=
XM_017015320.2:c.549A=	XP_016870809.1:p.Thr183=
XM_017015321.2:c.549A=	XP_016870810.1:p.Thr183=
XM_017015323.2:c.147A=	XP_016870812.1:p.Thr49=
XM_024447716.1:c.822A=	XP_024303484.1:p.Thr274=
XM_024447717.1:c.822A=	XP_024303485.1:p.Thr274=
XR_002956828.1:n.837A=
XR_002956829.1:n.837A=
XR_002956830.1:n.608A=
XR_002956831.1:n.283A=
XR_002956832.1:n.968A=
NM_012203.2:c.549A= MANE Select	NP_036335.1:p.Thr183=