Canonical Allele Identifier: CA14827015

Gene: MACROD2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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