Canonical Allele Identifier: CA2689982805

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37432165-C-CTCCCTGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432166_37432173dup , CM000671.2:g.37432166_37432173dup	GRCh38
NC_000009.11:g.37432163_37432170dup , CM000671.1:g.37432163_37432170dup	GRCh37
NC_000009.10:g.37422163_37422170dup	NCBI36
NG_008135.1:g.14457_14464dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.865+28_865+35dup MANE Select	ENSP00000313432.6:n.865+28_865+35dup
ENST00000318158.10:c.865+28_865+35dup	ENSP00000313432.6:n.865+28_865+35dup
ENST00000460882.5:n.892+28_892+35dup
ENST00000480596.5:n.1566+28_1566+35dup
ENST00000482603.1:n.318+28_318+35dup
ENST00000491488.5:n.570+28_570+35dup
ENST00000494290.1:c.*51+1015_*51+1022dup	ENSP00000432021.1:n.*51+1015_*51+1022dup
ENST00000497693.1:n.4433+28_4433+35dup
ENST00000512404.2:n.80_87dup
ENST00000607784.1:c.865+28_865+35dup	ENSP00000475569.1:n.865+28_865+35dup
NM_012203.1:c.865+28_865+35dup	NP_036335.1:n.865+28_865+35dup
XM_005251631.1:c.544+28_544+35dup	XP_005251688.1:n.544+28_544+35dup
XM_011518073.1:c.463+28_463+35dup	XP_011516375.1:n.463+28_463+35dup
XM_017015320.2:c.865+28_865+35dup	XP_016870809.1:n.865+28_865+35dup
XM_017015321.2:c.865+28_865+35dup	XP_016870810.1:n.865+28_865+35dup
XM_017015323.2:c.463+28_463+35dup	XP_016870812.1:n.463+28_463+35dup
XM_024447716.1:c.1138+28_1138+35dup	XP_024303484.1:n.1138+28_1138+35dup
XM_024447717.1:c.1138+28_1138+35dup	XP_024303485.1:n.1138+28_1138+35dup
XR_002956828.1:n.1153+28_1153+35dup
XR_002956829.1:n.1153+28_1153+35dup
XR_002956830.1:n.2285+28_2285+35dup
XR_002956831.1:n.1960+28_1960+35dup
XR_002956832.1:n.1284+28_1284+35dup
NM_012203.2:c.865+28_865+35dup MANE Select	NP_036335.1:n.865+28_865+35dup