Canonical Allele Identifier: CA1846874079

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432053_37432055delinsTGG , CM000671.2:g.37432053_37432055delinsTGG	GRCh38
NC_000009.11:g.37432050_37432052delinsTGG , CM000671.1:g.37432050_37432052delinsTGG	GRCh37
NC_000009.10:g.37422050_37422052delinsTGG	NCBI36
NG_008135.1:g.14344_14346delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.780_782delinsTGG MANE Select	ENSP00000313432.6:p.Ser260=
ENST00000318158.10:c.780_782delinsTGG	ENSP00000313432.6:p.Ser260=
ENST00000460882.5:n.807_809delinsTGG
ENST00000480596.5:n.1481_1483delinsTGG
ENST00000482603.1:n.233_235delinsTGG
ENST00000491488.5:n.485_487delinsTGG
ENST00000494290.1:c.*51+902_*51+904delinsTGG	ENSP00000432021.1:n.*51+902_*51+904delinsTGG
ENST00000497693.1:n.4348_4350delinsTGG
ENST00000607784.1:c.780_782delinsTGG	ENSP00000475569.1:p.Ser260=
NM_012203.1:c.780_782delinsTGG	NP_036335.1:p.Ser260=
XM_005251631.1:c.459_461delinsTGG	XP_005251688.1:p.Ser153=
XM_011518073.1:c.378_380delinsTGG	XP_011516375.1:p.Ser126=
XM_017015320.2:c.780_782delinsTGG	XP_016870809.1:p.Ser260=
XM_017015321.2:c.780_782delinsTGG	XP_016870810.1:p.Ser260=
XM_017015323.2:c.378_380delinsTGG	XP_016870812.1:p.Ser126=
XM_024447716.1:c.1053_1055delinsTGG	XP_024303484.1:p.Ser351=
XM_024447717.1:c.1053_1055delinsTGG	XP_024303485.1:p.Ser351=
XR_002956828.1:n.1068_1070delinsTGG
XR_002956829.1:n.1068_1070delinsTGG
XR_002956830.1:n.2200_2202delinsTGG
XR_002956831.1:n.1875_1877delinsTGG
XR_002956832.1:n.1199_1201delinsTGG
NM_012203.2:c.780_782delinsTGG MANE Select	NP_036335.1:p.Ser260=