Canonical Allele Identifier: CA2689952551

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37424833-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37424836del , CM000671.2:g.37424836del	GRCh38
NC_000009.11:g.37424833del , CM000671.1:g.37424833del	GRCh37
NC_000009.10:g.37414833del	NCBI36
NG_008135.1:g.7127del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.84-9del MANE Select	ENSP00000313432.6:n.84-9del
ENST00000318158.10:c.84-9del	ENSP00000313432.6:n.84-9del
ENST00000377824.8:n.121-9del
ENST00000460882.5:n.111-9del
ENST00000487399.5:n.93-9del
ENST00000491488.5:n.109+2003del
ENST00000493368.5:n.141-9del
ENST00000607784.1:c.84-9del	ENSP00000475569.1:n.84-9del
NM_012203.1:c.84-9del	NP_036335.1:n.84-9del
XM_005251631.1:c.83+2003del	XP_005251688.1:n.83+2003del
XM_011518073.1:c.-679-9del	XP_011516375.1:n.-679-9del
XR_929374.1:n.169-9del
XM_017015320.2:c.84-9del	XP_016870809.1:n.84-9del
XM_017015321.2:c.84-9del	XP_016870810.1:n.84-9del
XM_017015323.2:c.-679-9del	XP_016870812.1:n.-679-9del
XM_024447716.1:c.357-9del	XP_024303484.1:n.357-9del
XM_024447717.1:c.357-9del	XP_024303485.1:n.357-9del
XR_002956828.1:n.372-9del
XR_002956829.1:n.372-9del
XR_002956830.1:n.143-9del
XR_002956831.1:n.138+2003del
XR_002956832.1:n.143-9del
NM_012203.2:c.84-9del MANE Select	NP_036335.1:n.84-9del