Canonical Allele Identifier: CA1846869397

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428734C= , CM000671.2:g.37428734C=	GRCh38
NC_000009.11:g.37428731C= , CM000671.1:g.37428731C=	GRCh37
NC_000009.10:g.37418731C=	NCBI36
NG_008135.1:g.11025C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.493+162C= MANE Select	ENSP00000313432.6:n.493+162C=
ENST00000318158.10:c.493+162C=	ENSP00000313432.6:n.493+162C=
ENST00000377824.8:n.530+162C=
ENST00000460882.5:n.520+162C=
ENST00000480596.5:n.197C=
ENST00000491488.5:n.198+162C=
ENST00000493368.5:n.712C=
ENST00000497693.1:n.1029C=
ENST00000607784.1:c.493+162C=	ENSP00000475569.1:n.493+162C=
NM_012203.1:c.493+162C=	NP_036335.1:n.493+162C=
XM_005251631.1:c.172+162C=	XP_005251688.1:n.172+162C=
XM_011518073.1:c.-108C=	XP_011516375.1:n.-108C=
XR_929374.1:n.740C=
XM_017015320.2:c.493+162C=	XP_016870809.1:n.493+162C=
XM_017015321.2:c.493+162C=	XP_016870810.1:n.493+162C=
XM_017015323.2:c.-108C=	XP_016870812.1:n.-108C=
XM_024447716.1:c.766+162C=	XP_024303484.1:n.766+162C=
XM_024447717.1:c.766+162C=	XP_024303485.1:n.766+162C=
XR_002956828.1:n.781+162C=
XR_002956829.1:n.781+162C=
XR_002956830.1:n.552+162C=
XR_002956831.1:n.227+162C=
XR_002956832.1:n.714C=
NM_012203.2:c.493+162C= MANE Select	NP_036335.1:n.493+162C=