Canonical Allele Identifier: CA1846865097

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37425024C= , CM000671.2:g.37425024C=	GRCh38
NC_000009.11:g.37425021C= , CM000671.1:g.37425021C=	GRCh37
NC_000009.10:g.37415021C=	NCBI36
NG_008135.1:g.7315C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.214+49C= MANE Select	ENSP00000313432.6:n.214+49C=
ENST00000318158.10:c.214+49C=	ENSP00000313432.6:n.214+49C=
ENST00000377824.8:n.251+49C=
ENST00000460882.5:n.241+49C=
ENST00000487399.5:n.223+49C=
ENST00000491488.5:n.109+2191C=
ENST00000493368.5:n.271+49C=
ENST00000607784.1:c.214+49C=	ENSP00000475569.1:n.214+49C=
NM_012203.1:c.214+49C=	NP_036335.1:n.214+49C=
XM_005251631.1:c.83+2191C=	XP_005251688.1:n.83+2191C=
XM_011518073.1:c.-549+49C=	XP_011516375.1:n.-549+49C=
XR_929374.1:n.299+49C=
XM_017015320.2:c.214+49C=	XP_016870809.1:n.214+49C=
XM_017015321.2:c.214+49C=	XP_016870810.1:n.214+49C=
XM_017015323.2:c.-549+49C=	XP_016870812.1:n.-549+49C=
XM_024447716.1:c.487+49C=	XP_024303484.1:n.487+49C=
XM_024447717.1:c.487+49C=	XP_024303485.1:n.487+49C=
XR_002956828.1:n.502+49C=
XR_002956829.1:n.502+49C=
XR_002956830.1:n.273+49C=
XR_002956831.1:n.138+2191C=
XR_002956832.1:n.273+49C=
NM_012203.2:c.214+49C= MANE Select	NP_036335.1:n.214+49C=