Canonical Allele Identifier: CA1846870326

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429661_37429662delinsTC , CM000671.2:g.37429661_37429662delinsTC	GRCh38
NC_000009.11:g.37429658_37429659delinsTC , CM000671.1:g.37429658_37429659delinsTC	GRCh37
NC_000009.10:g.37419658_37419659delinsTC	NCBI36
NG_008135.1:g.11952_11953delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.494-71_494-70delinsTC MANE Select	ENSP00000313432.6:n.494-71_494-70delinsTC...
ENST00000318158.10:c.494-71_494-70delinsTC	ENSP00000313432.6:n.494-71_494-70delinsTC...
ENST00000377824.8:n.531-71_531-70delinsTC
ENST00000460882.5:n.521-71_521-70delinsTC
ENST00000480596.5:n.1124_1125delinsTC
ENST00000491488.5:n.199-71_199-70delinsTC
ENST00000494290.1:c.-7_-6delinsTC	ENSP00000432021.1:n.-7_-6delinsTC
ENST00000497693.1:n.1956_1957delinsTC
ENST00000607784.1:c.494-71_494-70delinsTC	ENSP00000475569.1:n.494-71_494-70delinsTC...
NM_012203.1:c.494-71_494-70delinsTC	NP_036335.1:n.494-71_494-70delinsTC
XM_005251631.1:c.173-71_173-70delinsTC	XP_005251688.1:n.173-71_173-70delinsTC
XM_011518073.1:c.92-71_92-70delinsTC	XP_011516375.1:n.92-71_92-70delinsTC
XR_929374.1:n.939-71_939-70delinsTC
XM_017015320.2:c.494-71_494-70delinsTC	XP_016870809.1:n.494-71_494-70delinsTC
XM_017015321.2:c.494-71_494-70delinsTC	XP_016870810.1:n.494-71_494-70delinsTC
XM_017015323.2:c.92-71_92-70delinsTC	XP_016870812.1:n.92-71_92-70delinsTC
XM_024447716.1:c.767-71_767-70delinsTC	XP_024303484.1:n.767-71_767-70delinsTC
XM_024447717.1:c.767-71_767-70delinsTC	XP_024303485.1:n.767-71_767-70delinsTC
XR_002956828.1:n.782-71_782-70delinsTC
XR_002956829.1:n.782-71_782-70delinsTC
XR_002956830.1:n.553-71_553-70delinsTC
XR_002956831.1:n.228-71_228-70delinsTC
XR_002956832.1:n.913-71_913-70delinsTC
NM_012203.2:c.494-71_494-70delinsTC MANE Select	NP_036335.1:n.494-71_494-70delinsTC