Canonical Allele Identifier: CA1692830158
Gene: MACC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20164143G= , CM000669.2:g.20164143G= GRCh38
NC_000007.13:g.20203766G= , CM000669.1:g.20203766G= GRCh37
NC_000007.12:g.20170291G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000400331.10:c.-9+113C= MANE Select ENSP00000383185.3:n.-9+113C=
ENST00000332878.8:c.-8-2273C= ENSP00000328410.4:n.-8-2273C=
ENST00000400331.9:c.-9+113C= ENSP00000383185.3:n.-9+113C=
ENST00000589011.1:c.-8-2273C= ENSP00000466864.1:n.-8-2273C=
NM_182762.3:c.-9+113C= NP_877439.3:n.-9+113C=
NM_182762.4:c.-9+113C= MANE Select NP_877439.3:n.-9+113C=