Canonical Allele Identifier: CA2579340805

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436860del , CM000671.2:g.37436860del	GRCh38
NC_000009.11:g.37436857del , CM000671.1:g.37436857del	GRCh37
NC_000009.10:g.37426857del	NCBI36
NG_008135.1:g.19151del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*78del MANE Select	ENSP00000313432.6:n.*78del
ENST00000318158.10:c.*78del	ENSP00000313432.6:n.*78del
ENST00000480596.5:n.1766del
ENST00000494290.1:c.*52-21del	ENSP00000432021.1:n.*52-21del
ENST00000497693.1:n.4633del
NM_012203.1:c.*78del	NP_036335.1:n.*78del
XM_005251631.1:c.*78del	XP_005251688.1:n.*78del
XM_011518073.1:c.*78del	XP_011516375.1:n.*78del
XM_017015320.2:c.946-551del	XP_016870809.1:n.946-551del
XM_017015321.2:c.866-551del	XP_016870810.1:n.866-551del
XM_017015323.2:c.544-551del	XP_016870812.1:n.544-551del
XM_024447716.1:c.1219-551del	XP_024303484.1:n.1219-551del
XM_024447717.1:c.1139-551del	XP_024303485.1:n.1139-551del
XR_002956828.1:n.1234-551del
XR_002956829.1:n.1154-551del
XR_002956830.1:n.2485del
XR_002956831.1:n.2160del
XR_002956832.1:n.1484del
NM_012203.2:c.*78del MANE Select	NP_036335.1:n.*78del