Canonical Allele Identifier: CA2580583511
Gene: MACO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25442446A>C , CM000663.2:g.25442446A>C GRCh38
NC_000001.10:g.25768937A>C , CM000663.1:g.25768937A>C GRCh37
NC_000001.9:g.25641524A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374343.5:c.81-4316A>C MANE Select ENSP00000363463.4:n.81-4316A>C
ENST00000647928.1:c.81-4316A>C ENSP00000497738.1:n.81-4316A>C
ENST00000374343.4:c.81-4316A>C ENSP00000363463.4:n.81-4316A>C
ENST00000399766.7:c.81-4316A>C ENSP00000382668.3:n.81-4316A>C
NM_001282564.1:c.81-4316A>C NP_001269493.1:n.81-4316A>C
NM_018202.5:c.81-4316A>C NP_060672.2:n.81-4316A>C
XM_005245931.1:c.81-4316A>C XP_005245988.1:n.81-4316A>C
XM_011541704.1:c.-531-4316A>C XP_011540006.1:n.-531-4316A>C
XM_005245931.2:c.81-4316A>C XP_005245988.1:n.81-4316A>C
XM_011541704.3:c.-531-4316A>C XP_011540006.1:n.-531-4316A>C
NM_018202.6:c.81-4316A>C MANE Select NP_060672.2:n.81-4316A>C
NM_001282564.2:c.81-4316A>C NP_001269493.1:n.81-4316A>C