Canonical Allele Identifier: CA1692830298
Gene: MACC1 HGNC NCBI

Linked Data

dbSNP Id: rs1782183186

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20164420del , CM000669.2:g.20164420del GRCh38
NC_000007.13:g.20204043del , CM000669.1:g.20204043del GRCh37
NC_000007.12:g.20170568del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000400331.10:c.-152-16del MANE Select ENSP00000383185.3:n.-152-16del
ENST00000332878.8:c.-8-2545del ENSP00000328410.4:n.-8-2545del
ENST00000400331.9:c.-152-16del ENSP00000383185.3:n.-152-16del
ENST00000471019.1:n.274-16del
ENST00000589011.1:c.-8-2545del ENSP00000466864.1:n.-8-2545del
NM_182762.3:c.-152-16del NP_877439.3:n.-152-16del
NM_182762.4:c.-152-16del MANE Select NP_877439.3:n.-152-16del