Canonical Allele Identifier: CA3165921350

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429753T= , CM000671.2:g.37429753T=	GRCh38
NC_000009.11:g.37429750T= , CM000671.1:g.37429750T=	GRCh37
NC_000009.10:g.37419750T=	NCBI36
NG_008135.1:g.12044T=

Transcript Alleles

HGVS	Amino-acid Change
NM_012203.2:c.515T= MANE Select	NP_036335.1:p.Leu172=
ENST00000318158.11:c.515T= MANE Select	ENSP00000313432.6:p.Leu172=
NM_012203.1:c.515T=	NP_036335.1:p.Leu172=
ENST00000318158.10:c.515T=	ENSP00000313432.6:p.Leu172=
ENST00000377824.8:n.552T=
ENST00000460882.5:n.542T=
ENST00000480596.5:n.1216T=
ENST00000491488.5:n.220T=
ENST00000494290.1:c.86T=	ENSP00000432021.1:p.Leu29=
ENST00000497693.1:n.2048T=
ENST00000607784.1:c.515T=	ENSP00000475569.1:p.Leu172=
XM_005251631.1:c.194T=	XP_005251688.1:p.Leu65=
XM_011518073.1:c.113T=	XP_011516375.1:p.Leu38=
XM_017015320.2:c.515T=	XP_016870809.1:p.Leu172=
XM_017015321.2:c.515T=	XP_016870810.1:p.Leu172=
XM_017015323.2:c.113T=	XP_016870812.1:p.Leu38=
XM_024447716.1:c.788T=	XP_024303484.1:p.Leu263=
XM_024447717.1:c.788T=	XP_024303485.1:p.Leu263=
XR_002956828.1:n.803T=
XR_002956829.1:n.803T=
XR_002956830.1:n.574T=
XR_002956831.1:n.249T=
XR_002956832.1:n.934T=
XR_929374.1:n.960T=