Canonical Allele Identifier: CA1846870516

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429770_37429772delinsCAG , CM000671.2:g.37429770_37429772delinsCAG	GRCh38
NC_000009.11:g.37429767_37429769delinsCAG , CM000671.1:g.37429767_37429769delinsCAG	GRCh37
NC_000009.10:g.37419767_37419769delinsCAG	NCBI36
NG_008135.1:g.12061_12063delinsCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.532_534delinsCAG MANE Select	ENSP00000313432.6:p.Gln178=
ENST00000318158.10:c.532_534delinsCAG	ENSP00000313432.6:p.Gln178=
ENST00000377824.8:n.569_571delinsCAG
ENST00000460882.5:n.559_561delinsCAG
ENST00000480596.5:n.1233_1235delinsCAG
ENST00000491488.5:n.237_239delinsCAG
ENST00000494290.1:c.103_105delinsCAG	ENSP00000432021.1:p.Gln35=
ENST00000497693.1:n.2065_2067delinsCAG
ENST00000607784.1:c.532_534delinsCAG	ENSP00000475569.1:p.Gln178=
NM_012203.1:c.532_534delinsCAG	NP_036335.1:p.Gln178=
XM_005251631.1:c.211_213delinsCAG	XP_005251688.1:p.Gln71=
XM_011518073.1:c.130_132delinsCAG	XP_011516375.1:p.Gln44=
XR_929374.1:n.977_979delinsCAG
XM_017015320.2:c.532_534delinsCAG	XP_016870809.1:p.Gln178=
XM_017015321.2:c.532_534delinsCAG	XP_016870810.1:p.Gln178=
XM_017015323.2:c.130_132delinsCAG	XP_016870812.1:p.Gln44=
XM_024447716.1:c.805_807delinsCAG	XP_024303484.1:p.Gln269=
XM_024447717.1:c.805_807delinsCAG	XP_024303485.1:p.Gln269=
XR_002956828.1:n.820_822delinsCAG
XR_002956829.1:n.820_822delinsCAG
XR_002956830.1:n.591_593delinsCAG
XR_002956831.1:n.266_268delinsCAG
XR_002956832.1:n.951_953delinsCAG
NM_012203.2:c.532_534delinsCAG MANE Select	NP_036335.1:p.Gln178=