Canonical Allele Identifier: CA2579340658

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428468_37428479del , CM000671.2:g.37428468_37428479del	GRCh38
NC_000009.11:g.37428465_37428476del , CM000671.1:g.37428465_37428476del	GRCh37
NC_000009.10:g.37418465_37418476del	NCBI36
NG_008135.1:g.10759_10770del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.405-16_405-5del MANE Select	ENSP00000313432.6:n.405-16_405-5del
ENST00000318158.10:c.405-16_405-5del	ENSP00000313432.6:n.405-16_405-5del
ENST00000377824.8:n.442-16_442-5del
ENST00000460882.5:n.432-16_432-5del
ENST00000491488.5:n.110-16_110-5del
ENST00000493368.5:n.462-16_462-5del
ENST00000497693.1:n.763_774del
ENST00000607784.1:c.405-16_405-5del	ENSP00000475569.1:n.405-16_405-5del
NM_012203.1:c.405-16_405-5del	NP_036335.1:n.405-16_405-5del
XM_005251631.1:c.84-16_84-5del	XP_005251688.1:n.84-16_84-5del
XM_011518073.1:c.-358-16_-358-5del	XP_011516375.1:n.-358-16_-358-5del
XR_929374.1:n.490-16_490-5del
XM_017015320.2:c.405-16_405-5del	XP_016870809.1:n.405-16_405-5del
XM_017015321.2:c.405-16_405-5del	XP_016870810.1:n.405-16_405-5del
XM_017015323.2:c.-358-16_-358-5del	XP_016870812.1:n.-358-16_-358-5del
XM_024447716.1:c.678-16_678-5del	XP_024303484.1:n.678-16_678-5del
XM_024447717.1:c.678-16_678-5del	XP_024303485.1:n.678-16_678-5del
XR_002956828.1:n.693-16_693-5del
XR_002956829.1:n.693-16_693-5del
XR_002956830.1:n.464-16_464-5del
XR_002956831.1:n.139-16_139-5del
XR_002956832.1:n.464-16_464-5del
NM_012203.2:c.405-16_405-5del MANE Select	NP_036335.1:n.405-16_405-5del