Canonical Allele Identifier: CA1846885478

Gene: GRHPR

Linked Data

• dbSNP Id: rs1823671127

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436652_37436654del , CM000671.2:g.37436652_37436654del	GRCh38
NC_000009.11:g.37436649_37436651del , CM000671.1:g.37436649_37436651del	GRCh37
NC_000009.10:g.37426649_37426651del	NCBI36
NG_008135.1:g.18943_18945del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.866-9_866-7del MANE Select	ENSP00000313432.6:n.866-9_866-7del
ENST00000318158.10:c.866-9_866-7del	ENSP00000313432.6:n.866-9_866-7del
ENST00000460882.5:n.893-9_893-7del
ENST00000480596.5:n.1567-9_1567-7del
ENST00000491488.5:n.571-9_571-7del
ENST00000494290.1:c.*52-229_*52-227del	ENSP00000432021.1:n.*52-229_*52-227del
ENST00000497693.1:n.4434-9_4434-7del
NM_012203.1:c.866-9_866-7del	NP_036335.1:n.866-9_866-7del
XM_005251631.1:c.545-9_545-7del	XP_005251688.1:n.545-9_545-7del
XM_011518073.1:c.464-9_464-7del	XP_011516375.1:n.464-9_464-7del
XM_017015320.2:c.946-759_946-757del	XP_016870809.1:n.946-759_946-757del
XM_017015321.2:c.866-759_866-757del	XP_016870810.1:n.866-759_866-757del
XM_017015323.2:c.544-759_544-757del	XP_016870812.1:n.544-759_544-757del
XM_024447716.1:c.1219-759_1219-757del	XP_024303484.1:n.1219-759_1219-757del
XM_024447717.1:c.1139-759_1139-757del	XP_024303485.1:n.1139-759_1139-757del
XR_002956828.1:n.1234-759_1234-757del
XR_002956829.1:n.1154-759_1154-757del
XR_002956830.1:n.2286-9_2286-7del
XR_002956831.1:n.1961-9_1961-7del
XR_002956832.1:n.1285-9_1285-7del
NM_012203.2:c.866-9_866-7del MANE Select	NP_036335.1:n.866-9_866-7del