Canonical Allele Identifier: CA2352013483

Gene: MACROD2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.15196934A= , CM000682.2:g.15196934A=	GRCh38
NC_000020.10:g.15177580A= , CM000682.1:g.15177580A=	GRCh37
NC_000020.9:g.15125580A=	NCBI36
NG_054905.1:g.1206435A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001351661.2:c.419-33006A= MANE Select	NP_001338590.1:n.419-33006A=
ENST00000684519.1:c.419-33006A= MANE Select	ENSP00000507484.1:n.419-33006A=
NM_001033087.1:c.-386A=	NP_001028259.1:n.-386A=
NM_001033087.2:c.-386A=	NP_001028259.1:n.-386A=
NM_001351661.1:c.419-33006A=	NP_001338590.1:n.419-33006A=
NM_001351663.1:c.419-33006A=	NP_001338592.1:n.419-33006A=
NM_001351663.2:c.419-33006A=	NP_001338592.1:n.419-33006A=
NM_001351664.1:c.-386A=	NP_001338593.1:n.-386A=
NM_001351664.2:c.-386A=	NP_001338593.1:n.-386A=
NM_080676.5:c.419-33006A=	NP_542407.2:n.419-33006A=
NM_080676.6:c.419-33006A=	NP_542407.2:n.419-33006A=
ENST00000217246.8:c.419-33006A=	ENSP00000217246.4:n.419-33006A=
ENST00000402914.5:c.-386A=	ENSP00000385290.1:n.-386A=
ENST00000642719.1:c.419-33006A=	ENSP00000496601.1:n.419-33006A=