Canonical Allele Identifier: CA1846870209

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429556G= , CM000671.2:g.37429556G=	GRCh38
NC_000009.11:g.37429553G= , CM000671.1:g.37429553G=	GRCh37
NC_000009.10:g.37419553G=	NCBI36
NG_008135.1:g.11847G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.494-176G= MANE Select	ENSP00000313432.6:n.494-176G=
ENST00000318158.10:c.494-176G=	ENSP00000313432.6:n.494-176G=
ENST00000377824.8:n.531-176G=
ENST00000460882.5:n.521-176G=
ENST00000480596.5:n.1019G=
ENST00000491488.5:n.199-176G=
ENST00000494290.1:c.-112G=	ENSP00000432021.1:n.-112G=
ENST00000497693.1:n.1851G=
ENST00000607784.1:c.494-176G=	ENSP00000475569.1:n.494-176G=
NM_012203.1:c.494-176G=	NP_036335.1:n.494-176G=
XM_005251631.1:c.173-176G=	XP_005251688.1:n.173-176G=
XM_011518073.1:c.92-176G=	XP_011516375.1:n.92-176G=
XR_929374.1:n.939-176G=
XM_017015320.2:c.494-176G=	XP_016870809.1:n.494-176G=
XM_017015321.2:c.494-176G=	XP_016870810.1:n.494-176G=
XM_017015323.2:c.92-176G=	XP_016870812.1:n.92-176G=
XM_024447716.1:c.767-176G=	XP_024303484.1:n.767-176G=
XM_024447717.1:c.767-176G=	XP_024303485.1:n.767-176G=
XR_002956828.1:n.782-176G=
XR_002956829.1:n.782-176G=
XR_002956830.1:n.553-176G=
XR_002956831.1:n.228-176G=
XR_002956832.1:n.913-176G=
NM_012203.2:c.494-176G= MANE Select	NP_036335.1:n.494-176G=