Canonical Allele Identifier: CA1846885137

Gene: GRHPR

Linked Data

• dbSNP Id: rs1823660854

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436561_37436562del , CM000671.2:g.37436561_37436562del	GRCh38
NC_000009.11:g.37436558_37436559del , CM000671.1:g.37436558_37436559del	GRCh37
NC_000009.10:g.37426558_37426559del	NCBI36
NG_008135.1:g.18852_18853del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-100_866-99del MANE Select	ENSP00000313432.6:n.866-100_866-99del
ENST00000318158.10:c.866-100_866-99del	ENSP00000313432.6:n.866-100_866-99del
ENST00000460882.5:n.893-100_893-99del
ENST00000480596.5:n.1567-100_1567-99del
ENST00000491488.5:n.571-100_571-99del
ENST00000494290.1:c.*52-320_*52-319del	ENSP00000432021.1:n.*52-320_*52-319del
ENST00000497693.1:n.4434-100_4434-99del
NM_012203.1:c.866-100_866-99del	NP_036335.1:n.866-100_866-99del
XM_005251631.1:c.545-100_545-99del	XP_005251688.1:n.545-100_545-99del
XM_011518073.1:c.464-100_464-99del	XP_011516375.1:n.464-100_464-99del
XM_017015320.2:c.946-850_946-849del	XP_016870809.1:n.946-850_946-849del
XM_017015321.2:c.866-850_866-849del	XP_016870810.1:n.866-850_866-849del
XM_017015323.2:c.544-850_544-849del	XP_016870812.1:n.544-850_544-849del
XM_024447716.1:c.1219-850_1219-849del	XP_024303484.1:n.1219-850_1219-849del
XM_024447717.1:c.1139-850_1139-849del	XP_024303485.1:n.1139-850_1139-849del
XR_002956828.1:n.1234-850_1234-849del
XR_002956829.1:n.1154-850_1154-849del
XR_002956830.1:n.2286-100_2286-99del
XR_002956831.1:n.1961-100_1961-99del
XR_002956832.1:n.1285-100_1285-99del
NM_012203.2:c.866-100_866-99del MANE Select	NP_036335.1:n.866-100_866-99del