Canonical Allele Identifier: CA106766225
Gene: MAML3 HGNC NCBI

Linked Data

dbSNP Id: rs35897758
MyVariant Identifiers: chr4:g.140795197_140795198insC (hg19) chr4:g.139874043_139874044insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.139874044dup , CM000666.2:g.139874044dup GRCh38
NC_000004.11:g.140795198dup , CM000666.1:g.140795198dup GRCh37
NC_000004.10:g.141014648dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502696.1:c.111-143377dup
ENST00000509479.6:c.2079+15313dup MANE Select ENSP00000421180.1:n.2079+15313dup
NM_018717.4:c.2067+15313dup NP_061187.2:n.2067+15313dup
NM_018717.5:c.2079+15313dup MANE Select NP_061187.3:n.2079+15313dup
Search 100 bp 5'
Search 100 bp 3'