Canonical Allele Identifier: CA1099112672
Gene: MACC1 HGNC NCBI

Linked Data

dbSNP Id: rs1782183086
gnomAD v3: 7-20164413-AG-A
gnomAD v4: 7-20164413-AG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20164414del , CM000669.2:g.20164414del GRCh38
NC_000007.13:g.20204037del , CM000669.1:g.20204037del GRCh37
NC_000007.12:g.20170562del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000400331.10:c.-152-15del MANE Select ENSP00000383185.3:n.-152-15del
ENST00000332878.8:c.-8-2544del ENSP00000328410.4:n.-8-2544del
ENST00000400331.9:c.-152-15del ENSP00000383185.3:n.-152-15del
ENST00000471019.1:n.274-15del
ENST00000589011.1:c.-8-2544del ENSP00000466864.1:n.-8-2544del
NM_182762.3:c.-152-15del NP_877439.3:n.-152-15del
NM_182762.4:c.-152-15del MANE Select NP_877439.3:n.-152-15del
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