Canonical Allele Identifier: CA1846874391

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432143G= , CM000671.2:g.37432143G=	GRCh38
NC_000009.11:g.37432140G= , CM000671.1:g.37432140G=	GRCh37
NC_000009.10:g.37422140G=	NCBI36
NG_008135.1:g.14434G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.865+5G= MANE Select	ENSP00000313432.6:n.865+5G=
ENST00000318158.10:c.865+5G=	ENSP00000313432.6:n.865+5G=
ENST00000460882.5:n.892+5G=
ENST00000480596.5:n.1566+5G=
ENST00000482603.1:n.318+5G=
ENST00000491488.5:n.570+5G=
ENST00000494290.1:c.*51+992G=	ENSP00000432021.1:n.*51+992G=
ENST00000497693.1:n.4433+5G=
ENST00000512404.2:n.57G=
ENST00000607784.1:c.865+5G=	ENSP00000475569.1:n.865+5G=
NM_012203.1:c.865+5G=	NP_036335.1:n.865+5G=
XM_005251631.1:c.544+5G=	XP_005251688.1:n.544+5G=
XM_011518073.1:c.463+5G=	XP_011516375.1:n.463+5G=
XM_017015320.2:c.865+5G=	XP_016870809.1:n.865+5G=
XM_017015321.2:c.865+5G=	XP_016870810.1:n.865+5G=
XM_017015323.2:c.463+5G=	XP_016870812.1:n.463+5G=
XM_024447716.1:c.1138+5G=	XP_024303484.1:n.1138+5G=
XM_024447717.1:c.1138+5G=	XP_024303485.1:n.1138+5G=
XR_002956828.1:n.1153+5G=
XR_002956829.1:n.1153+5G=
XR_002956830.1:n.2285+5G=
XR_002956831.1:n.1960+5G=
XR_002956832.1:n.1284+5G=
NM_012203.2:c.865+5G= MANE Select	NP_036335.1:n.865+5G=