Canonical Allele Identifier: CA16041328
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37428514_37428515del , CM000671.2:g.37428514_37428515del GRCh38
NC_000009.11:g.37428511_37428512del , CM000671.1:g.37428511_37428512del GRCh37
NC_000009.10:g.37418511_37418512del NCBI36
NG_008135.1:g.10805_10806del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318158.11:c.435_436del MANE Select ENSP00000313432.6:p.Trp145CysfsTer?
ENST00000318158.10:c.435_436del ENSP00000313432.6:p.Trp145CysfsTer?
ENST00000377824.8:n.472_473del
ENST00000460882.5:n.462_463del
ENST00000491488.5:n.140_141del
ENST00000493368.5:n.492_493del
ENST00000497693.1:n.809_810del
ENST00000607784.1:c.435_436del ENSP00000475569.1:p.Trp145CysfsTer?
NM_012203.1:c.435_436del NP_036335.1:p.Trp145CysfsTer?
XM_005251631.1:c.114_115del XP_005251688.1:p.Trp38CysfsTer?
XM_011518073.1:c.-328_-327del XP_011516375.1:n.-328_-327del
XR_929374.1:n.520_521del
XM_017015320.2:c.435_436del XP_016870809.1:p.Trp145CysfsTer?
XM_017015321.2:c.435_436del XP_016870810.1:p.Trp145CysfsTer?
XM_017015323.2:c.-328_-327del XP_016870812.1:n.-328_-327del
XM_024447716.1:c.708_709del XP_024303484.1:p.Trp236CysfsTer?
XM_024447717.1:c.708_709del XP_024303485.1:p.Trp236CysfsTer?
XR_002956828.1:n.723_724del
XR_002956829.1:n.723_724del
XR_002956830.1:n.494_495del
XR_002956831.1:n.169_170del
XR_002956832.1:n.494_495del
NM_012203.2:c.435_436del MANE Select NP_036335.1:p.Trp145CysfsTer?