Canonical Allele Identifier: CA1692830201
Gene: MACC1 HGNC NCBI

Linked Data

dbSNP Id: rs1782179691
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20164237_20164238insCCCCCGGCCC , CM000669.2:g.20164237_20164238insCCCCCGGCCC GRCh38
NC_000007.13:g.20203860_20203861insCCCCCGGCCC , CM000669.1:g.20203860_20203861insCCCCCGGCCC GRCh37
NC_000007.12:g.20170385_20170386insCCCCCGGCCC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000400331.10:c.-9+26_-9+27insGGGGGCCGGG MANE Select ENSP00000383185.3:n.-9+26_-9+27insGGGGGCCGGG
ENST00000332878.8:c.-8-2360_-8-2359insGGGGGCCGGG ENSP00000328410.4:n.-8-2360_-8-2359insGGGGGCCGGG
ENST00000400331.9:c.-9+26_-9+27insGGGGGCCGGG ENSP00000383185.3:n.-9+26_-9+27insGGGGGCCGGG
ENST00000589011.1:c.-8-2360_-8-2359insGGGGGCCGGG ENSP00000466864.1:n.-8-2360_-8-2359insGGGGGCCGGG
NM_182762.3:c.-9+26_-9+27insGGGGGCCGGG NP_877439.3:n.-9+26_-9+27insGGGGGCCGGG
NM_182762.4:c.-9+26_-9+27insGGGGGCCGGG MANE Select NP_877439.3:n.-9+26_-9+27insGGGGGCCGGG
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