Canonical Allele Identifier: CA1846869450

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428799_37428800delinsTA , CM000671.2:g.37428799_37428800delinsTA	GRCh38
NC_000009.11:g.37428796_37428797delinsTA , CM000671.1:g.37428796_37428797delinsTA	GRCh37
NC_000009.10:g.37418796_37418797delinsTA	NCBI36
NG_008135.1:g.11090_11091delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.493+227_493+228delinsTA MANE Select	ENSP00000313432.6:n.493+227_493+228delinsTA
ENST00000318158.10:c.493+227_493+228delinsTA	ENSP00000313432.6:n.493+227_493+228delinsTA
ENST00000377824.8:n.530+227_530+228delinsTA
ENST00000460882.5:n.520+227_520+228delinsTA
ENST00000480596.5:n.262_263delinsTA
ENST00000491488.5:n.198+227_198+228delinsTA
ENST00000493368.5:n.777_778delinsTA
ENST00000497693.1:n.1094_1095delinsTA
ENST00000607784.1:c.493+227_493+228delinsTA	ENSP00000475569.1:n.493+227_493+228delinsTA
NM_012203.1:c.493+227_493+228delinsTA	NP_036335.1:n.493+227_493+228delinsTA
XM_005251631.1:c.172+227_172+228delinsTA	XP_005251688.1:n.172+227_172+228delinsTA
XM_011518073.1:c.-43_-42delinsTA	XP_011516375.1:n.-43_-42delinsTA
XR_929374.1:n.805_806delinsTA
XM_017015320.2:c.493+227_493+228delinsTA	XP_016870809.1:n.493+227_493+228delinsTA
XM_017015321.2:c.493+227_493+228delinsTA	XP_016870810.1:n.493+227_493+228delinsTA
XM_017015323.2:c.-43_-42delinsTA	XP_016870812.1:n.-43_-42delinsTA
XM_024447716.1:c.766+227_766+228delinsTA	XP_024303484.1:n.766+227_766+228delinsTA
XM_024447717.1:c.766+227_766+228delinsTA	XP_024303485.1:n.766+227_766+228delinsTA
XR_002956828.1:n.781+227_781+228delinsTA
XR_002956829.1:n.781+227_781+228delinsTA
XR_002956830.1:n.552+227_552+228delinsTA
XR_002956831.1:n.227+227_227+228delinsTA
XR_002956832.1:n.779_780delinsTA
NM_012203.2:c.493+227_493+228delinsTA MANE Select	NP_036335.1:n.493+227_493+228delinsTA