Canonical Allele Identifier: CA1846869408

Gene: GRHPR

Linked Data

• dbSNP Id: rs1823209162

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428746_37428749del , CM000671.2:g.37428746_37428749del	GRCh38
NC_000009.11:g.37428743_37428746del , CM000671.1:g.37428743_37428746del	GRCh37
NC_000009.10:g.37418743_37418746del	NCBI36
NG_008135.1:g.11037_11040del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.493+174_493+177del MANE Select	ENSP00000313432.6:n.493+174_493+177del
ENST00000318158.10:c.493+174_493+177del	ENSP00000313432.6:n.493+174_493+177del
ENST00000377824.8:n.530+174_530+177del
ENST00000460882.5:n.520+174_520+177del
ENST00000480596.5:n.209_212del
ENST00000491488.5:n.198+174_198+177del
ENST00000493368.5:n.724_727del
ENST00000497693.1:n.1041_1044del
ENST00000607784.1:c.493+174_493+177del	ENSP00000475569.1:n.493+174_493+177del
NM_012203.1:c.493+174_493+177del	NP_036335.1:n.493+174_493+177del
XM_005251631.1:c.172+174_172+177del	XP_005251688.1:n.172+174_172+177del
XM_011518073.1:c.-96_-93del	XP_011516375.1:n.-96_-93del
XR_929374.1:n.752_755del
XM_017015320.2:c.493+174_493+177del	XP_016870809.1:n.493+174_493+177del
XM_017015321.2:c.493+174_493+177del	XP_016870810.1:n.493+174_493+177del
XM_017015323.2:c.-96_-93del	XP_016870812.1:n.-96_-93del
XM_024447716.1:c.766+174_766+177del	XP_024303484.1:n.766+174_766+177del
XM_024447717.1:c.766+174_766+177del	XP_024303485.1:n.766+174_766+177del
XR_002956828.1:n.781+174_781+177del
XR_002956829.1:n.781+174_781+177del
XR_002956830.1:n.552+174_552+177del
XR_002956831.1:n.227+174_227+177del
XR_002956832.1:n.726_729del
NM_012203.2:c.493+174_493+177del MANE Select	NP_036335.1:n.493+174_493+177del