Canonical Allele Identifier: CA1846868884

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428446_37428447delinsAG , CM000671.2:g.37428446_37428447delinsAG	GRCh38
NC_000009.11:g.37428443_37428444delinsAG , CM000671.1:g.37428443_37428444delinsAG	GRCh37
NC_000009.10:g.37418443_37418444delinsAG	NCBI36
NG_008135.1:g.10737_10738delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.405-38_405-37delinsAG MANE Select	ENSP00000313432.6:n.405-38_405-37delinsAG
ENST00000318158.10:c.405-38_405-37delinsAG	ENSP00000313432.6:n.405-38_405-37delinsAG
ENST00000377824.8:n.442-38_442-37delinsAG
ENST00000460882.5:n.432-38_432-37delinsAG
ENST00000491488.5:n.110-38_110-37delinsAG
ENST00000493368.5:n.462-38_462-37delinsAG
ENST00000497693.1:n.741_742delinsAG
ENST00000607784.1:c.405-38_405-37delinsAG	ENSP00000475569.1:n.405-38_405-37delinsAG
NM_012203.1:c.405-38_405-37delinsAG	NP_036335.1:n.405-38_405-37delinsAG
XM_005251631.1:c.84-38_84-37delinsAG	XP_005251688.1:n.84-38_84-37delinsAG
XM_011518073.1:c.-358-38_-358-37delinsAG	XP_011516375.1:n.-358-38_-358-37delinsAG
XR_929374.1:n.490-38_490-37delinsAG
XM_017015320.2:c.405-38_405-37delinsAG	XP_016870809.1:n.405-38_405-37delinsAG
XM_017015321.2:c.405-38_405-37delinsAG	XP_016870810.1:n.405-38_405-37delinsAG
XM_017015323.2:c.-358-38_-358-37delinsAG	XP_016870812.1:n.-358-38_-358-37delinsAG
XM_024447716.1:c.678-38_678-37delinsAG	XP_024303484.1:n.678-38_678-37delinsAG
XM_024447717.1:c.678-38_678-37delinsAG	XP_024303485.1:n.678-38_678-37delinsAG
XR_002956828.1:n.693-38_693-37delinsAG
XR_002956829.1:n.693-38_693-37delinsAG
XR_002956830.1:n.464-38_464-37delinsAG
XR_002956831.1:n.139-38_139-37delinsAG
XR_002956832.1:n.464-38_464-37delinsAG
NM_012203.2:c.405-38_405-37delinsAG MANE Select	NP_036335.1:n.405-38_405-37delinsAG