Canonical Allele Identifier: CA1846887132

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436981_37436983delinsTTC , CM000671.2:g.37436981_37436983delinsTTC	GRCh38
NC_000009.11:g.37436978_37436980delinsTTC , CM000671.1:g.37436978_37436980delinsTTC	GRCh37
NC_000009.10:g.37426978_37426980delinsTTC	NCBI36
NG_008135.1:g.19272_19274delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*199_*201delinsTTC MANE Select	ENSP00000313432.6:n.*199_*201delinsTTC
ENST00000318158.10:c.*199_*201delinsTTC	ENSP00000313432.6:n.*199_*201delinsTTC
ENST00000480596.5:n.1887_1889delinsTTC
ENST00000494290.1:c.*152_*154delinsTTC	ENSP00000432021.1:n.*152_*154delinsTTC
ENST00000497693.1:n.4754_4756delinsTTC
NM_012203.1:c.*199_*201delinsTTC	NP_036335.1:n.*199_*201delinsTTC
XM_005251631.1:c.*199_*201delinsTTC	XP_005251688.1:n.*199_*201delinsTTC
XM_011518073.1:c.*199_*201delinsTTC	XP_011516375.1:n.*199_*201delinsTTC
XM_017015320.2:c.946-430_946-428delinsTTC	XP_016870809.1:n.946-430_946-428delinsTTC
XM_017015321.2:c.866-430_866-428delinsTTC	XP_016870810.1:n.866-430_866-428delinsTTC
XM_017015323.2:c.544-430_544-428delinsTTC	XP_016870812.1:n.544-430_544-428delinsTTC
XM_024447716.1:c.1219-430_1219-428delinsTTC	XP_024303484.1:n.1219-430_1219-428delinsTTC
XM_024447717.1:c.1139-430_1139-428delinsTTC	XP_024303485.1:n.1139-430_1139-428delinsTTC
XR_002956828.1:n.1234-430_1234-428delinsTTC
XR_002956829.1:n.1154-430_1154-428delinsTTC
XR_002956830.1:n.2606_2608delinsTTC
XR_002956831.1:n.2281_2283delinsTTC
XR_002956832.1:n.1605_1607delinsTTC
NM_012203.2:c.*199_*201delinsTTC MANE Select	NP_036335.1:n.*199_*201delinsTTC