Canonical Allele Identifier: CA1846865657

Gene: GRHPR

Linked Data

• dbSNP Id: rs1823051847
• gnomAD v4: 9-37425855-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37425856_37425857del , CM000671.2:g.37425856_37425857del	GRCh38
NC_000009.11:g.37425853_37425854del , CM000671.1:g.37425853_37425854del	GRCh37
NC_000009.10:g.37415853_37415854del	NCBI36
NG_008135.1:g.8147_8148del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.215-66_215-65del MANE Select	ENSP00000313432.6:n.215-66_215-65del
ENST00000318158.10:c.215-66_215-65del	ENSP00000313432.6:n.215-66_215-65del
ENST00000377824.8:n.252-66_252-65del
ENST00000460882.5:n.242-66_242-65del
ENST00000487399.5:n.224-66_224-65del
ENST00000491488.5:n.110-2628_110-2627del
ENST00000493368.5:n.272-66_272-65del
ENST00000607784.1:c.215-66_215-65del	ENSP00000475569.1:n.215-66_215-65del
NM_012203.1:c.215-66_215-65del	NP_036335.1:n.215-66_215-65del
XM_005251631.1:c.84-2628_84-2627del	XP_005251688.1:n.84-2628_84-2627del
XM_011518073.1:c.-548-66_-548-65del	XP_011516375.1:n.-548-66_-548-65del
XR_929374.1:n.300-66_300-65del
XM_017015320.2:c.215-66_215-65del	XP_016870809.1:n.215-66_215-65del
XM_017015321.2:c.215-66_215-65del	XP_016870810.1:n.215-66_215-65del
XM_017015323.2:c.-548-66_-548-65del	XP_016870812.1:n.-548-66_-548-65del
XM_024447716.1:c.488-66_488-65del	XP_024303484.1:n.488-66_488-65del
XM_024447717.1:c.488-66_488-65del	XP_024303485.1:n.488-66_488-65del
XR_002956828.1:n.503-66_503-65del
XR_002956829.1:n.503-66_503-65del
XR_002956830.1:n.274-66_274-65del
XR_002956831.1:n.139-2628_139-2627del
XR_002956832.1:n.274-66_274-65del
NM_012203.2:c.215-66_215-65del MANE Select	NP_036335.1:n.215-66_215-65del