Canonical Allele Identifier: CA1846869456

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428806_37428807delinsCA , CM000671.2:g.37428806_37428807delinsCA	GRCh38
NC_000009.11:g.37428803_37428804delinsCA , CM000671.1:g.37428803_37428804delinsCA	GRCh37
NC_000009.10:g.37418803_37418804delinsCA	NCBI36
NG_008135.1:g.11097_11098delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.493+234_493+235delinsCA MANE Select	ENSP00000313432.6:n.493+234_493+235delinsCA
ENST00000318158.10:c.493+234_493+235delinsCA	ENSP00000313432.6:n.493+234_493+235delinsCA
ENST00000377824.8:n.530+234_530+235delinsCA
ENST00000460882.5:n.520+234_520+235delinsCA
ENST00000480596.5:n.269_270delinsCA
ENST00000491488.5:n.198+234_198+235delinsCA
ENST00000493368.5:n.784_785delinsCA
ENST00000497693.1:n.1101_1102delinsCA
ENST00000607784.1:c.493+234_493+235delinsCA	ENSP00000475569.1:n.493+234_493+235delinsCA
NM_012203.1:c.493+234_493+235delinsCA	NP_036335.1:n.493+234_493+235delinsCA
XM_005251631.1:c.172+234_172+235delinsCA	XP_005251688.1:n.172+234_172+235delinsCA
XM_011518073.1:c.-36_-35delinsCA	XP_011516375.1:n.-36_-35delinsCA
XR_929374.1:n.812_813delinsCA
XM_017015320.2:c.493+234_493+235delinsCA	XP_016870809.1:n.493+234_493+235delinsCA
XM_017015321.2:c.493+234_493+235delinsCA	XP_016870810.1:n.493+234_493+235delinsCA
XM_017015323.2:c.-36_-35delinsCA	XP_016870812.1:n.-36_-35delinsCA
XM_024447716.1:c.766+234_766+235delinsCA	XP_024303484.1:n.766+234_766+235delinsCA
XM_024447717.1:c.766+234_766+235delinsCA	XP_024303485.1:n.766+234_766+235delinsCA
XR_002956828.1:n.781+234_781+235delinsCA
XR_002956829.1:n.781+234_781+235delinsCA
XR_002956830.1:n.552+234_552+235delinsCA
XR_002956831.1:n.227+234_227+235delinsCA
XR_002956832.1:n.786_787delinsCA
NM_012203.2:c.493+234_493+235delinsCA MANE Select	NP_036335.1:n.493+234_493+235delinsCA