Canonical Allele Identifier: CA1846885350

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436633_37436635delinsTCC , CM000671.2:g.37436633_37436635delinsTCC	GRCh38
NC_000009.11:g.37436630_37436632delinsTCC , CM000671.1:g.37436630_37436632delinsTCC	GRCh37
NC_000009.10:g.37426630_37426632delinsTCC	NCBI36
NG_008135.1:g.18924_18926delinsTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-28_866-26delinsTCC MANE Select	ENSP00000313432.6:n.866-28_866-26delinsTCC
ENST00000318158.10:c.866-28_866-26delinsTCC	ENSP00000313432.6:n.866-28_866-26delinsTCC
ENST00000460882.5:n.893-28_893-26delinsTCC
ENST00000480596.5:n.1567-28_1567-26delinsTCC
ENST00000491488.5:n.571-28_571-26delinsTCC
ENST00000494290.1:c.*52-248_*52-246delinsTCC	ENSP00000432021.1:n.*52-248_*52-246delinsTCC
ENST00000497693.1:n.4434-28_4434-26delinsTCC
NM_012203.1:c.866-28_866-26delinsTCC	NP_036335.1:n.866-28_866-26delinsTCC
XM_005251631.1:c.545-28_545-26delinsTCC	XP_005251688.1:n.545-28_545-26delinsTCC
XM_011518073.1:c.464-28_464-26delinsTCC	XP_011516375.1:n.464-28_464-26delinsTCC
XM_017015320.2:c.946-778_946-776delinsTCC	XP_016870809.1:n.946-778_946-776delinsTCC
XM_017015321.2:c.866-778_866-776delinsTCC	XP_016870810.1:n.866-778_866-776delinsTCC
XM_017015323.2:c.544-778_544-776delinsTCC	XP_016870812.1:n.544-778_544-776delinsTCC
XM_024447716.1:c.1219-778_1219-776delinsTCC	XP_024303484.1:n.1219-778_1219-776delinsTCC
XM_024447717.1:c.1139-778_1139-776delinsTCC	XP_024303485.1:n.1139-778_1139-776delinsTCC
XR_002956828.1:n.1234-778_1234-776delinsTCC
XR_002956829.1:n.1154-778_1154-776delinsTCC
XR_002956830.1:n.2286-28_2286-26delinsTCC
XR_002956831.1:n.1961-28_1961-26delinsTCC
XR_002956832.1:n.1285-28_1285-26delinsTCC
NM_012203.2:c.866-28_866-26delinsTCC MANE Select	NP_036335.1:n.866-28_866-26delinsTCC