Canonical Allele Identifier: CA2689982854

Gene: GRHPR

Linked Data

• gnomAD v4: 9-37432235-CAGGTGTTGAACCCAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432239_37432253del , CM000671.2:g.37432239_37432253del	GRCh38
NC_000009.11:g.37432236_37432250del , CM000671.1:g.37432236_37432250del	GRCh37
NC_000009.10:g.37422236_37422250del	NCBI36
NG_008135.1:g.14530_14544del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.865+101_865+115del MANE Select	ENSP00000313432.6:n.865+101_865+115del
ENST00000318158.10:c.865+101_865+115del	ENSP00000313432.6:n.865+101_865+115del
ENST00000460882.5:n.892+101_892+115del
ENST00000480596.5:n.1566+101_1566+115del
ENST00000482603.1:n.318+101_318+115del
ENST00000491488.5:n.570+101_570+115del
ENST00000494290.1:c.*51+1088_*51+1102del	ENSP00000432021.1:n.*51+1088_*51+1102del
ENST00000497693.1:n.4433+101_4433+115del
ENST00000512404.2:n.153_167del
ENST00000607784.1:c.865+101_865+115del	ENSP00000475569.1:n.865+101_865+115del
NM_012203.1:c.865+101_865+115del	NP_036335.1:n.865+101_865+115del
XM_005251631.1:c.544+101_544+115del	XP_005251688.1:n.544+101_544+115del
XM_011518073.1:c.463+101_463+115del	XP_011516375.1:n.463+101_463+115del
XM_017015320.2:c.865+101_865+115del	XP_016870809.1:n.865+101_865+115del
XM_017015321.2:c.865+101_865+115del	XP_016870810.1:n.865+101_865+115del
XM_017015323.2:c.463+101_463+115del	XP_016870812.1:n.463+101_463+115del
XM_024447716.1:c.1138+101_1138+115del	XP_024303484.1:n.1138+101_1138+115del
XM_024447717.1:c.1138+101_1138+115del	XP_024303485.1:n.1138+101_1138+115del
XR_002956828.1:n.1153+101_1153+115del
XR_002956829.1:n.1153+101_1153+115del
XR_002956830.1:n.2285+101_2285+115del
XR_002956831.1:n.1960+101_1960+115del
XR_002956832.1:n.1284+101_1284+115del
NM_012203.2:c.865+101_865+115del MANE Select	NP_036335.1:n.865+101_865+115del