Canonical Allele Identifier: CA2351647263
Community Standard Title: NM_001351661.2(MACROD2):c.272-85910C=
Gene: MACROD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.14407569C= , CM000682.2:g.14407569C= GRCh38
NC_000020.10:g.14388215C= , CM000682.1:g.14388215C= GRCh37
NC_000020.9:g.14336215C= NCBI36
NG_054905.1:g.417070C=

Transcript Alleles

HGVS Amino-acid Change
NM_001351661.2:c.272-85910C= MANE Select NP_001338590.1:n.272-85910C=
ENST00000684519.1:c.272-85910C= MANE Select ENSP00000507484.1:n.272-85910C=
NM_001351661.1:c.272-85910C= NP_001338590.1:n.272-85910C=
NM_001351663.1:c.272-85910C= NP_001338592.1:n.272-85910C=
NM_001351663.2:c.272-85910C= NP_001338592.1:n.272-85910C=
NM_080676.5:c.272-85910C= NP_542407.2:n.272-85910C=
NM_080676.6:c.272-85910C= NP_542407.2:n.272-85910C=
ENST00000217246.8:c.272-85910C= ENSP00000217246.4:n.272-85910C=
ENST00000477147.5:n.541-85910C=
ENST00000490428.5:n.263-85910C=
ENST00000494602.5:n.299-85910C=
ENST00000642719.1:c.272-85910C= ENSP00000496601.1:n.272-85910C=