Canonical Allele Identifier: CA1846870548

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429790G= , CM000671.2:g.37429790G=	GRCh38
NC_000009.11:g.37429787G= , CM000671.1:g.37429787G=	GRCh37
NC_000009.10:g.37419787G=	NCBI36
NG_008135.1:g.12081G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.552G= MANE Select	ENSP00000313432.6:p.Gly184=
ENST00000318158.10:c.552G=	ENSP00000313432.6:p.Gly184=
ENST00000377824.8:n.589G=
ENST00000460882.5:n.579G=
ENST00000480596.5:n.1253G=
ENST00000482603.1:n.5G=
ENST00000491488.5:n.257G=
ENST00000494290.1:c.123G=	ENSP00000432021.1:p.Gly41=
ENST00000497693.1:n.2085G=
ENST00000607784.1:c.552G=	ENSP00000475569.1:p.Gly184=
NM_012203.1:c.552G=	NP_036335.1:p.Gly184=
XM_005251631.1:c.231G=	XP_005251688.1:p.Gly77=
XM_011518073.1:c.150G=	XP_011516375.1:p.Gly50=
XR_929374.1:n.997G=
XM_017015320.2:c.552G=	XP_016870809.1:p.Gly184=
XM_017015321.2:c.552G=	XP_016870810.1:p.Gly184=
XM_017015323.2:c.150G=	XP_016870812.1:p.Gly50=
XM_024447716.1:c.825G=	XP_024303484.1:p.Gly275=
XM_024447717.1:c.825G=	XP_024303485.1:p.Gly275=
XR_002956828.1:n.840G=
XR_002956829.1:n.840G=
XR_002956830.1:n.611G=
XR_002956831.1:n.286G=
XR_002956832.1:n.971G=
NM_012203.2:c.552G= MANE Select	NP_036335.1:p.Gly184=