Canonical Allele Identifier: CA1846870358

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429670_37429683delinsGCTGGGTGGTGTCC , CM000671.2:g.37429670_37429683delinsGCTGGGTGGTGTCC	GRCh38
NC_000009.11:g.37429667_37429680delinsGCTGGGTGGTGTCC , CM000671.1:g.37429667_37429680delinsGCTGGGTGGTGTCC	GRCh37
NC_000009.10:g.37419667_37419680delinsGCTGGGTGGTGTCC	NCBI36
NG_008135.1:g.11961_11974delinsGCTGGGTGGTGTCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.494-62_494-49delinsGCTGGGTGGTGTCC MANE Select	ENSP00000313432.6:n.494-62_494-49delinsGC...
ENST00000318158.10:c.494-62_494-49delinsGCTGGGTGGTGTCC	ENSP00000313432.6:n.494-62_494-49delinsGC...
ENST00000377824.8:n.531-62_531-49delinsGCTGGGTGGTGTCC
ENST00000460882.5:n.521-62_521-49delinsGCTGGGTGGTGTCC
ENST00000480596.5:n.1133_1146delinsGCTGGGTGGTGTCC
ENST00000491488.5:n.199-62_199-49delinsGCTGGGTGGTGTCC
ENST00000494290.1:c.3_16delinsGCTGGGTGGTGTCC	ENSP00000432021.1:p.Met1=
ENST00000497693.1:n.1965_1978delinsGCTGGGTGGTGTCC
ENST00000607784.1:c.494-62_494-49delinsGCTGGGTGGTGTCC	ENSP00000475569.1:n.494-62_494-49delinsGC...
NM_012203.1:c.494-62_494-49delinsGCTGGGTGGTGTCC	NP_036335.1:n.494-62_494-49delinsGCTGGGTG...
XM_005251631.1:c.173-62_173-49delinsGCTGGGTGGTGTCC	XP_005251688.1:n.173-62_173-49delinsGCTGG...
XM_011518073.1:c.92-62_92-49delinsGCTGGGTGGTGTCC	XP_011516375.1:n.92-62_92-49delinsGCTGGGT...
XR_929374.1:n.939-62_939-49delinsGCTGGGTGGTGTCC
XM_017015320.2:c.494-62_494-49delinsGCTGGGTGGTGTCC	XP_016870809.1:n.494-62_494-49delinsGCTGG...
XM_017015321.2:c.494-62_494-49delinsGCTGGGTGGTGTCC	XP_016870810.1:n.494-62_494-49delinsGCTGG...
XM_017015323.2:c.92-62_92-49delinsGCTGGGTGGTGTCC	XP_016870812.1:n.92-62_92-49delinsGCTGGGT...
XM_024447716.1:c.767-62_767-49delinsGCTGGGTGGTGTCC	XP_024303484.1:n.767-62_767-49delinsGCTGG...
XM_024447717.1:c.767-62_767-49delinsGCTGGGTGGTGTCC	XP_024303485.1:n.767-62_767-49delinsGCTGG...
XR_002956828.1:n.782-62_782-49delinsGCTGGGTGGTGTCC
XR_002956829.1:n.782-62_782-49delinsGCTGGGTGGTGTCC
XR_002956830.1:n.553-62_553-49delinsGCTGGGTGGTGTCC
XR_002956831.1:n.228-62_228-49delinsGCTGGGTGGTGTCC
XR_002956832.1:n.913-62_913-49delinsGCTGGGTGGTGTCC
NM_012203.2:c.494-62_494-49delinsGCTGGGTGGTGTCC MANE Select	NP_036335.1:n.494-62_494-49delinsGCTGGGTG...