Canonical Allele Identifier: CA2351620384
Community Standard Title: NM_001351661.2(MACROD2):c.272-146226G=
Gene: MACROD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.14347253G= , CM000682.2:g.14347253G= GRCh38
NC_000020.10:g.14327899G= , CM000682.1:g.14327899G= GRCh37
NC_000020.9:g.14275899G= NCBI36
NG_054905.1:g.356754G=

Transcript Alleles

HGVS Amino-acid Change
NM_001351661.2:c.272-146226G= MANE Select NP_001338590.1:n.272-146226G=
ENST00000684519.1:c.272-146226G= MANE Select ENSP00000507484.1:n.272-146226G=
NM_001351661.1:c.272-146226G= NP_001338590.1:n.272-146226G=
NM_001351663.1:c.272-146226G= NP_001338592.1:n.272-146226G=
NM_001351663.2:c.272-146226G= NP_001338592.1:n.272-146226G=
NM_080676.5:c.272-146226G= NP_542407.2:n.272-146226G=
NM_080676.6:c.272-146226G= NP_542407.2:n.272-146226G=
ENST00000217246.8:c.272-146226G= ENSP00000217246.4:n.272-146226G=
ENST00000477147.5:n.541-146226G=
ENST00000490428.5:n.263-146226G=
ENST00000494602.5:n.299-146226G=
ENST00000642719.1:c.272-146226G= ENSP00000496601.1:n.272-146226G=