Canonical Allele Identifier: CA1846868911

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428464G= , CM000671.2:g.37428464G=	GRCh38
NC_000009.11:g.37428461G= , CM000671.1:g.37428461G=	GRCh37
NC_000009.10:g.37418461G=	NCBI36
NG_008135.1:g.10755G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.405-20G= MANE Select	ENSP00000313432.6:n.405-20G=
ENST00000318158.10:c.405-20G=	ENSP00000313432.6:n.405-20G=
ENST00000377824.8:n.442-20G=
ENST00000460882.5:n.432-20G=
ENST00000491488.5:n.110-20G=
ENST00000493368.5:n.462-20G=
ENST00000497693.1:n.759G=
ENST00000607784.1:c.405-20G=	ENSP00000475569.1:n.405-20G=
NM_012203.1:c.405-20G=	NP_036335.1:n.405-20G=
XM_005251631.1:c.84-20G=	XP_005251688.1:n.84-20G=
XM_011518073.1:c.-358-20G=	XP_011516375.1:n.-358-20G=
XR_929374.1:n.490-20G=
XM_017015320.2:c.405-20G=	XP_016870809.1:n.405-20G=
XM_017015321.2:c.405-20G=	XP_016870810.1:n.405-20G=
XM_017015323.2:c.-358-20G=	XP_016870812.1:n.-358-20G=
XM_024447716.1:c.678-20G=	XP_024303484.1:n.678-20G=
XM_024447717.1:c.678-20G=	XP_024303485.1:n.678-20G=
XR_002956828.1:n.693-20G=
XR_002956829.1:n.693-20G=
XR_002956830.1:n.464-20G=
XR_002956831.1:n.139-20G=
XR_002956832.1:n.464-20G=
NM_012203.2:c.405-20G= MANE Select	NP_036335.1:n.405-20G=