Canonical Allele Identifier: CA1846869459

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428807_37428808delinsAG , CM000671.2:g.37428807_37428808delinsAG	GRCh38
NC_000009.11:g.37428804_37428805delinsAG , CM000671.1:g.37428804_37428805delinsAG	GRCh37
NC_000009.10:g.37418804_37418805delinsAG	NCBI36
NG_008135.1:g.11098_11099delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.493+235_493+236delinsAG MANE Select	ENSP00000313432.6:n.493+235_493+236delinsAG
ENST00000318158.10:c.493+235_493+236delinsAG	ENSP00000313432.6:n.493+235_493+236delinsAG
ENST00000377824.8:n.530+235_530+236delinsAG
ENST00000460882.5:n.520+235_520+236delinsAG
ENST00000480596.5:n.270_271delinsAG
ENST00000491488.5:n.198+235_198+236delinsAG
ENST00000493368.5:n.785_786delinsAG
ENST00000497693.1:n.1102_1103delinsAG
ENST00000607784.1:c.493+235_493+236delinsAG	ENSP00000475569.1:n.493+235_493+236delinsAG
NM_012203.1:c.493+235_493+236delinsAG	NP_036335.1:n.493+235_493+236delinsAG
XM_005251631.1:c.172+235_172+236delinsAG	XP_005251688.1:n.172+235_172+236delinsAG
XM_011518073.1:c.-35_-34delinsAG	XP_011516375.1:n.-35_-34delinsAG
XR_929374.1:n.813_814delinsAG
XM_017015320.2:c.493+235_493+236delinsAG	XP_016870809.1:n.493+235_493+236delinsAG
XM_017015321.2:c.493+235_493+236delinsAG	XP_016870810.1:n.493+235_493+236delinsAG
XM_017015323.2:c.-35_-34delinsAG	XP_016870812.1:n.-35_-34delinsAG
XM_024447716.1:c.766+235_766+236delinsAG	XP_024303484.1:n.766+235_766+236delinsAG
XM_024447717.1:c.766+235_766+236delinsAG	XP_024303485.1:n.766+235_766+236delinsAG
XR_002956828.1:n.781+235_781+236delinsAG
XR_002956829.1:n.781+235_781+236delinsAG
XR_002956830.1:n.552+235_552+236delinsAG
XR_002956831.1:n.227+235_227+236delinsAG
XR_002956832.1:n.787_788delinsAG
NM_012203.2:c.493+235_493+236delinsAG MANE Select	NP_036335.1:n.493+235_493+236delinsAG