Canonical Allele Identifier: CA2689981356

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37429868-ATCTGTGCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429869_37429876del , CM000671.2:g.37429869_37429876del	GRCh38
NC_000009.11:g.37429866_37429873del , CM000671.1:g.37429866_37429873del	GRCh37
NC_000009.10:g.37419866_37419873del	NCBI36
NG_008135.1:g.12160_12167del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.598+33_598+40del MANE Select	ENSP00000313432.6:n.598+33_598+40del
ENST00000318158.10:c.598+33_598+40del	ENSP00000313432.6:n.598+33_598+40del
ENST00000377824.8:n.635+33_635+40del
ENST00000460882.5:n.625+33_625+40del
ENST00000480596.5:n.1299+33_1299+40del
ENST00000482603.1:n.51+33_51+40del
ENST00000491488.5:n.303+33_303+40del
ENST00000494290.1:c.169+33_169+40del	ENSP00000432021.1:n.169+33_169+40del
ENST00000497693.1:n.2164_2171del
ENST00000607784.1:c.598+33_598+40del	ENSP00000475569.1:n.598+33_598+40del
NM_012203.1:c.598+33_598+40del	NP_036335.1:n.598+33_598+40del
XM_005251631.1:c.277+33_277+40del	XP_005251688.1:n.277+33_277+40del
XM_011518073.1:c.196+33_196+40del	XP_011516375.1:n.196+33_196+40del
XR_929374.1:n.1043+33_1043+40del
XM_017015320.2:c.598+33_598+40del	XP_016870809.1:n.598+33_598+40del
XM_017015321.2:c.598+33_598+40del	XP_016870810.1:n.598+33_598+40del
XM_017015323.2:c.196+33_196+40del	XP_016870812.1:n.196+33_196+40del
XM_024447716.1:c.871+33_871+40del	XP_024303484.1:n.871+33_871+40del
XM_024447717.1:c.871+33_871+40del	XP_024303485.1:n.871+33_871+40del
XR_002956828.1:n.886+33_886+40del
XR_002956829.1:n.886+33_886+40del
XR_002956830.1:n.657+33_657+40del
XR_002956831.1:n.332+33_332+40del
XR_002956832.1:n.1017+33_1017+40del
NM_012203.2:c.598+33_598+40del MANE Select	NP_036335.1:n.598+33_598+40del