Canonical Allele Identifier: CA2554233098

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429654_37429655insAGA , CM000671.2:g.37429654_37429655insAGA	GRCh38
NC_000009.11:g.37429651_37429652insAGA , CM000671.1:g.37429651_37429652insAGA	GRCh37
NC_000009.10:g.37419651_37419652insAGA	NCBI36
NG_008135.1:g.11945_11946insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.494-78_494-77insAGA MANE Select	ENSP00000313432.6:n.494-78_494-77insAGA
ENST00000318158.10:c.494-78_494-77insAGA	ENSP00000313432.6:n.494-78_494-77insAGA
ENST00000377824.8:n.531-78_531-77insAGA
ENST00000460882.5:n.521-78_521-77insAGA
ENST00000480596.5:n.1117_1118insAGA
ENST00000491488.5:n.199-78_199-77insAGA
ENST00000494290.1:c.-14_-13insAGA	ENSP00000432021.1:n.-14_-13insAGA
ENST00000497693.1:n.1949_1950insAGA
ENST00000607784.1:c.494-78_494-77insAGA	ENSP00000475569.1:n.494-78_494-77insAGA
NM_012203.1:c.494-78_494-77insAGA	NP_036335.1:n.494-78_494-77insAGA
XM_005251631.1:c.173-78_173-77insAGA	XP_005251688.1:n.173-78_173-77insAGA
XM_011518073.1:c.92-78_92-77insAGA	XP_011516375.1:n.92-78_92-77insAGA
XR_929374.1:n.939-78_939-77insAGA
XM_017015320.2:c.494-78_494-77insAGA	XP_016870809.1:n.494-78_494-77insAGA
XM_017015321.2:c.494-78_494-77insAGA	XP_016870810.1:n.494-78_494-77insAGA
XM_017015323.2:c.92-78_92-77insAGA	XP_016870812.1:n.92-78_92-77insAGA
XM_024447716.1:c.767-78_767-77insAGA	XP_024303484.1:n.767-78_767-77insAGA
XM_024447717.1:c.767-78_767-77insAGA	XP_024303485.1:n.767-78_767-77insAGA
XR_002956828.1:n.782-78_782-77insAGA
XR_002956829.1:n.782-78_782-77insAGA
XR_002956830.1:n.553-78_553-77insAGA
XR_002956831.1:n.228-78_228-77insAGA
XR_002956832.1:n.913-78_913-77insAGA
NM_012203.2:c.494-78_494-77insAGA MANE Select	NP_036335.1:n.494-78_494-77insAGA