Canonical Allele Identifier: CA1692830168
Gene: MACC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20164160C= , CM000669.2:g.20164160C= GRCh38
NC_000007.13:g.20203783C= , CM000669.1:g.20203783C= GRCh37
NC_000007.12:g.20170308C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000400331.10:c.-9+96G= MANE Select ENSP00000383185.3:n.-9+96G=
ENST00000332878.8:c.-8-2290G= ENSP00000328410.4:n.-8-2290G=
ENST00000400331.9:c.-9+96G= ENSP00000383185.3:n.-9+96G=
ENST00000589011.1:c.-8-2290G= ENSP00000466864.1:n.-8-2290G=
NM_182762.3:c.-9+96G= NP_877439.3:n.-9+96G=
NM_182762.4:c.-9+96G= MANE Select NP_877439.3:n.-9+96G=