Canonical Allele Identifier: CA1692830150
Gene: MACC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20164128G= , CM000669.2:g.20164128G= GRCh38
NC_000007.13:g.20203751G= , CM000669.1:g.20203751G= GRCh37
NC_000007.12:g.20170276G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000400331.10:c.-9+128C= MANE Select ENSP00000383185.3:n.-9+128C=
ENST00000332878.8:c.-8-2258C= ENSP00000328410.4:n.-8-2258C=
ENST00000400331.9:c.-9+128C= ENSP00000383185.3:n.-9+128C=
ENST00000589011.1:c.-8-2258C= ENSP00000466864.1:n.-8-2258C=
NM_182762.3:c.-9+128C= NP_877439.3:n.-9+128C=
NM_182762.4:c.-9+128C= MANE Select NP_877439.3:n.-9+128C=