Canonical Allele Identifier: CA836505595
Gene: MACC1 HGNC NCBI

Linked Data

dbSNP Id: rs1425810928
gnomAD v3: 7-20164255-CT-C
gnomAD v4: 7-20164255-CT-C
MyVariant Identifiers: chr7:g.20203879del (hg19) chr7:g.20164256del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20164260del , CM000669.2:g.20164260del GRCh38
NC_000007.13:g.20203883del , CM000669.1:g.20203883del GRCh37
NC_000007.12:g.20170408del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000400331.10:c.-9del MANE Select ENSP00000383185.3:n.-9del
ENST00000332878.8:c.-8-2386del ENSP00000328410.4:n.-8-2386del
ENST00000400331.9:c.-9del ENSP00000383185.3:n.-9del
ENST00000589011.1:c.-8-2386del ENSP00000466864.1:n.-8-2386del
NM_182762.3:c.-9del NP_877439.3:n.-9del
NM_182762.4:c.-9del MANE Select NP_877439.3:n.-9del
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