Canonical Allele Identifier: CA863757681

Gene: GRHPR

Linked Data

• dbSNP Id: rs1284512161
• gnomAD v4: 9-37425875-TGAGTTCCTC-T
• MyVariant Identifiers: chr9:g.37425873_37425881del (hg19) ; chr9:g.37425876_37425884del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37425879_37425887del , CM000671.2:g.37425879_37425887del	GRCh38
NC_000009.11:g.37425876_37425884del , CM000671.1:g.37425876_37425884del	GRCh37
NC_000009.10:g.37415876_37415884del	NCBI36
NG_008135.1:g.8170_8178del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.215-43_215-35del MANE Select	ENSP00000313432.6:n.215-43_215-35del
ENST00000318158.10:c.215-43_215-35del	ENSP00000313432.6:n.215-43_215-35del
ENST00000377824.8:n.252-43_252-35del
ENST00000460882.5:n.242-43_242-35del
ENST00000487399.5:n.224-43_224-35del
ENST00000491488.5:n.110-2605_110-2597del
ENST00000493368.5:n.272-43_272-35del
ENST00000607784.1:c.215-43_215-35del	ENSP00000475569.1:n.215-43_215-35del
NM_012203.1:c.215-43_215-35del	NP_036335.1:n.215-43_215-35del
XM_005251631.1:c.84-2605_84-2597del	XP_005251688.1:n.84-2605_84-2597del
XM_011518073.1:c.-548-43_-548-35del	XP_011516375.1:n.-548-43_-548-35del
XR_929374.1:n.300-43_300-35del
XM_017015320.2:c.215-43_215-35del	XP_016870809.1:n.215-43_215-35del
XM_017015321.2:c.215-43_215-35del	XP_016870810.1:n.215-43_215-35del
XM_017015323.2:c.-548-43_-548-35del	XP_016870812.1:n.-548-43_-548-35del
XM_024447716.1:c.488-43_488-35del	XP_024303484.1:n.488-43_488-35del
XM_024447717.1:c.488-43_488-35del	XP_024303485.1:n.488-43_488-35del
XR_002956828.1:n.503-43_503-35del
XR_002956829.1:n.503-43_503-35del
XR_002956830.1:n.274-43_274-35del
XR_002956831.1:n.139-2605_139-2597del
XR_002956832.1:n.274-43_274-35del
NM_012203.2:c.215-43_215-35del MANE Select	NP_036335.1:n.215-43_215-35del