Canonical Allele Identifier: CA1846869347

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428706T= , CM000671.2:g.37428706T=	GRCh38
NC_000009.11:g.37428703T= , CM000671.1:g.37428703T=	GRCh37
NC_000009.10:g.37418703T=	NCBI36
NG_008135.1:g.10997T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.493+134T= MANE Select	ENSP00000313432.6:n.493+134T=
ENST00000318158.10:c.493+134T=	ENSP00000313432.6:n.493+134T=
ENST00000377824.8:n.530+134T=
ENST00000460882.5:n.520+134T=
ENST00000480596.5:n.169T=
ENST00000491488.5:n.198+134T=
ENST00000493368.5:n.684T=
ENST00000497693.1:n.1001T=
ENST00000607784.1:c.493+134T=	ENSP00000475569.1:n.493+134T=
NM_012203.1:c.493+134T=	NP_036335.1:n.493+134T=
XM_005251631.1:c.172+134T=	XP_005251688.1:n.172+134T=
XM_011518073.1:c.-136T=	XP_011516375.1:n.-136T=
XR_929374.1:n.712T=
XM_017015320.2:c.493+134T=	XP_016870809.1:n.493+134T=
XM_017015321.2:c.493+134T=	XP_016870810.1:n.493+134T=
XM_017015323.2:c.-136T=	XP_016870812.1:n.-136T=
XM_024447716.1:c.766+134T=	XP_024303484.1:n.766+134T=
XM_024447717.1:c.766+134T=	XP_024303485.1:n.766+134T=
XR_002956828.1:n.781+134T=
XR_002956829.1:n.781+134T=
XR_002956830.1:n.552+134T=
XR_002956831.1:n.227+134T=
XR_002956832.1:n.686T=
NM_012203.2:c.493+134T= MANE Select	NP_036335.1:n.493+134T=