Canonical Allele Identifier: CA1846870501

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429757A= , CM000671.2:g.37429757A=	GRCh38
NC_000009.11:g.37429754A= , CM000671.1:g.37429754A=	GRCh37
NC_000009.10:g.37419754A=	NCBI36
NG_008135.1:g.12048A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.519A= MANE Select	ENSP00000313432.6:p.Lys173=
ENST00000318158.10:c.519A=	ENSP00000313432.6:p.Lys173=
ENST00000377824.8:n.556A=
ENST00000460882.5:n.546A=
ENST00000480596.5:n.1220A=
ENST00000491488.5:n.224A=
ENST00000494290.1:c.90A=	ENSP00000432021.1:p.Lys30=
ENST00000497693.1:n.2052A=
ENST00000607784.1:c.519A=	ENSP00000475569.1:p.Lys173=
NM_012203.1:c.519A=	NP_036335.1:p.Lys173=
XM_005251631.1:c.198A=	XP_005251688.1:p.Lys66=
XM_011518073.1:c.117A=	XP_011516375.1:p.Lys39=
XR_929374.1:n.964A=
XM_017015320.2:c.519A=	XP_016870809.1:p.Lys173=
XM_017015321.2:c.519A=	XP_016870810.1:p.Lys173=
XM_017015323.2:c.117A=	XP_016870812.1:p.Lys39=
XM_024447716.1:c.792A=	XP_024303484.1:p.Lys264=
XM_024447717.1:c.792A=	XP_024303485.1:p.Lys264=
XR_002956828.1:n.807A=
XR_002956829.1:n.807A=
XR_002956830.1:n.578A=
XR_002956831.1:n.253A=
XR_002956832.1:n.938A=
NM_012203.2:c.519A= MANE Select	NP_036335.1:p.Lys173=