Canonical Allele Identifier: CA1846865065

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37424988_37424989delinsTG , CM000671.2:g.37424988_37424989delinsTG	GRCh38
NC_000009.11:g.37424985_37424986delinsTG , CM000671.1:g.37424985_37424986delinsTG	GRCh37
NC_000009.10:g.37414985_37414986delinsTG	NCBI36
NG_008135.1:g.7279_7280delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.214+13_214+14delinsTG MANE Select	ENSP00000313432.6:n.214+13_214+14delinsTG
ENST00000318158.10:c.214+13_214+14delinsTG	ENSP00000313432.6:n.214+13_214+14delinsTG
ENST00000377824.8:n.251+13_251+14delinsTG
ENST00000460882.5:n.241+13_241+14delinsTG
ENST00000487399.5:n.223+13_223+14delinsTG
ENST00000491488.5:n.109+2155_109+2156delinsTG
ENST00000493368.5:n.271+13_271+14delinsTG
ENST00000607784.1:c.214+13_214+14delinsTG	ENSP00000475569.1:n.214+13_214+14delinsTG
NM_012203.1:c.214+13_214+14delinsTG	NP_036335.1:n.214+13_214+14delinsTG
XM_005251631.1:c.83+2155_83+2156delinsTG	XP_005251688.1:n.83+2155_83+2156delinsTG
XM_011518073.1:c.-549+13_-549+14delinsTG	XP_011516375.1:n.-549+13_-549+14delinsTG
XR_929374.1:n.299+13_299+14delinsTG
XM_017015320.2:c.214+13_214+14delinsTG	XP_016870809.1:n.214+13_214+14delinsTG
XM_017015321.2:c.214+13_214+14delinsTG	XP_016870810.1:n.214+13_214+14delinsTG
XM_017015323.2:c.-549+13_-549+14delinsTG	XP_016870812.1:n.-549+13_-549+14delinsTG
XM_024447716.1:c.487+13_487+14delinsTG	XP_024303484.1:n.487+13_487+14delinsTG
XM_024447717.1:c.487+13_487+14delinsTG	XP_024303485.1:n.487+13_487+14delinsTG
XR_002956828.1:n.502+13_502+14delinsTG
XR_002956829.1:n.502+13_502+14delinsTG
XR_002956830.1:n.273+13_273+14delinsTG
XR_002956831.1:n.138+2155_138+2156delinsTG
XR_002956832.1:n.273+13_273+14delinsTG
NM_012203.2:c.214+13_214+14delinsTG MANE Select	NP_036335.1:n.214+13_214+14delinsTG