Canonical Allele Identifier: CA2333119599
Community Standard Title: NM_014686.5(GARRE1):c.-796+21069G=
Gene: GARRE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.34275683G= , CM000681.2:g.34275683G= GRCh38
NC_000019.9:g.34766588G= , CM000681.1:g.34766588G= GRCh37
NC_000019.8:g.39458428G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_014686.5:c.-796+21069G= MANE Select NP_055501.2:n.-796+21069G=
ENST00000299505.8:c.-796+21069G= MANE Select ENSP00000299505.4:n.-796+21069G=
NM_014686.3:c.-796+21069G= NP_055501.2:n.-796+21069G=
NM_014686.4:c.-796+21069G= NP_055501.2:n.-796+21069G=
ENST00000299505.6:c.-796+21069G= ENSP00000299505.4:n.-796+21069G=
ENST00000585833.1:n.55-9467G=
ENST00000588338.6:n.18+21069G=
ENST00000588470.5:c.-337+21069G= ENSP00000475249.1:n.-337+21069G=
ENST00000589583.5:c.-455+21069G= ENSP00000465362.1:n.-455+21069G=
ENST00000592124.1:n.64+10062G=
XM_005259444.1:c.-796+10062G= XP_005259501.1:n.-796+10062G=
XM_017027525.2:c.-796+21069G= XP_016883014.1:n.-796+21069G=