Canonical Allele Identifier: CA1846887140

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436986_37436988delinsTGA , CM000671.2:g.37436986_37436988delinsTGA	GRCh38
NC_000009.11:g.37436983_37436985delinsTGA , CM000671.1:g.37436983_37436985delinsTGA	GRCh37
NC_000009.10:g.37426983_37426985delinsTGA	NCBI36
NG_008135.1:g.19277_19279delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*204_*206delinsTGA MANE Select	ENSP00000313432.6:n.*204_*206delinsTGA
ENST00000318158.10:c.*204_*206delinsTGA	ENSP00000313432.6:n.*204_*206delinsTGA
ENST00000494290.1:c.*157_*159delinsTGA	ENSP00000432021.1:n.*157_*159delinsTGA
ENST00000497693.1:n.4759_4761delinsTGA
NM_012203.1:c.*204_*206delinsTGA	NP_036335.1:n.*204_*206delinsTGA
XM_005251631.1:c.*204_*206delinsTGA	XP_005251688.1:n.*204_*206delinsTGA
XM_011518073.1:c.*204_*206delinsTGA	XP_011516375.1:n.*204_*206delinsTGA
XM_017015320.2:c.946-425_946-423delinsTGA	XP_016870809.1:n.946-425_946-423delinsTGA
XM_017015321.2:c.866-425_866-423delinsTGA	XP_016870810.1:n.866-425_866-423delinsTGA
XM_017015323.2:c.544-425_544-423delinsTGA	XP_016870812.1:n.544-425_544-423delinsTGA
XM_024447716.1:c.1219-425_1219-423delinsTGA	XP_024303484.1:n.1219-425_1219-423delinsTGA
XM_024447717.1:c.1139-425_1139-423delinsTGA	XP_024303485.1:n.1139-425_1139-423delinsTGA
XR_002956828.1:n.1234-425_1234-423delinsTGA
XR_002956829.1:n.1154-425_1154-423delinsTGA
XR_002956830.1:n.2611_2613delinsTGA
XR_002956831.1:n.2286_2288delinsTGA
XR_002956832.1:n.1610_1612delinsTGA
NM_012203.2:c.*204_*206delinsTGA MANE Select	NP_036335.1:n.*204_*206delinsTGA