Canonical Allele Identifier: CA1846870644

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429837_37429838delinsGT , CM000671.2:g.37429837_37429838delinsGT	GRCh38
NC_000009.11:g.37429834_37429835delinsGT , CM000671.1:g.37429834_37429835delinsGT	GRCh37
NC_000009.10:g.37419834_37419835delinsGT	NCBI36
NG_008135.1:g.12128_12129delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.598+1_598+2delinsGT MANE Select	ENSP00000313432.6:n.598+1_598+2delinsGT
ENST00000318158.10:c.598+1_598+2delinsGT	ENSP00000313432.6:n.598+1_598+2delinsGT
ENST00000377824.8:n.635+1_635+2delinsGT
ENST00000460882.5:n.625+1_625+2delinsGT
ENST00000480596.5:n.1299+1_1299+2delinsGT
ENST00000482603.1:n.51+1_51+2delinsGT
ENST00000491488.5:n.303+1_303+2delinsGT
ENST00000494290.1:c.169+1_169+2delinsGT	ENSP00000432021.1:n.169+1_169+2delinsGT
ENST00000497693.1:n.2132_2133delinsGT
ENST00000607784.1:c.598+1_598+2delinsGT	ENSP00000475569.1:n.598+1_598+2delinsGT
NM_012203.1:c.598+1_598+2delinsGT	NP_036335.1:n.598+1_598+2delinsGT
XM_005251631.1:c.277+1_277+2delinsGT	XP_005251688.1:n.277+1_277+2delinsGT
XM_011518073.1:c.196+1_196+2delinsGT	XP_011516375.1:n.196+1_196+2delinsGT
XR_929374.1:n.1043+1_1043+2delinsGT
XM_017015320.2:c.598+1_598+2delinsGT	XP_016870809.1:n.598+1_598+2delinsGT
XM_017015321.2:c.598+1_598+2delinsGT	XP_016870810.1:n.598+1_598+2delinsGT
XM_017015323.2:c.196+1_196+2delinsGT	XP_016870812.1:n.196+1_196+2delinsGT
XM_024447716.1:c.871+1_871+2delinsGT	XP_024303484.1:n.871+1_871+2delinsGT
XM_024447717.1:c.871+1_871+2delinsGT	XP_024303485.1:n.871+1_871+2delinsGT
XR_002956828.1:n.886+1_886+2delinsGT
XR_002956829.1:n.886+1_886+2delinsGT
XR_002956830.1:n.657+1_657+2delinsGT
XR_002956831.1:n.332+1_332+2delinsGT
XR_002956832.1:n.1017+1_1017+2delinsGT
NM_012203.2:c.598+1_598+2delinsGT MANE Select	NP_036335.1:n.598+1_598+2delinsGT