Canonical Allele Identifier: CA1692830308
Gene: MACC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20164439_20164441delinsCAG , CM000669.2:g.20164439_20164441delinsCAG GRCh38
NC_000007.13:g.20204062_20204064delinsCAG , CM000669.1:g.20204062_20204064delinsCAG GRCh37
NC_000007.12:g.20170587_20170589delinsCAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000400331.10:c.-152-42_-152-40delinsCTG MANE Select ENSP00000383185.3:n.-152-42_-152-40delinsCTG
ENST00000332878.8:c.-8-2571_-8-2569delinsCTG ENSP00000328410.4:n.-8-2571_-8-2569delinsCTG
ENST00000400331.9:c.-152-42_-152-40delinsCTG ENSP00000383185.3:n.-152-42_-152-40delinsCTG
ENST00000471019.1:n.274-42_274-40delinsCTG
ENST00000589011.1:c.-8-2571_-8-2569delinsCTG ENSP00000466864.1:n.-8-2571_-8-2569delinsCTG
NM_182762.3:c.-152-42_-152-40delinsCTG NP_877439.3:n.-152-42_-152-40delinsCTG
NM_182762.4:c.-152-42_-152-40delinsCTG MANE Select NP_877439.3:n.-152-42_-152-40delinsCTG