Canonical Allele Identifier: CA366916949

Gene: MACC1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20158817G>T , CM000669.2:g.20158817G>T	GRCh38
NC_000007.13:g.20198440G>T , CM000669.1:g.20198440G>T	GRCh37
NC_000007.12:g.20164965G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400331.10:c.1544C>A MANE Select	ENSP00000383185.3:p.Ser515Ter
ENST00000332878.8:c.1544C>A	ENSP00000328410.4:p.Ser515Ter
ENST00000400331.9:c.1544C>A	ENSP00000383185.3:p.Ser515Ter
ENST00000589011.1:c.1544C>A	ENSP00000466864.1:p.Ser515Ter
NM_182762.3:c.1544C>A	NP_877439.3:p.Ser515Ter
NM_182762.4:c.1544C>A MANE Select	NP_877439.3:p.Ser515Ter