Canonical Allele Identifier: CA1584518738
Gene: TIFAB HGNC NCBI
DCANP1 HGNC NCBI

Linked Data

dbSNP Id: rs1769236871
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135445325C>T , CM000667.2:g.135445325C>T GRCh38
NC_000005.9:g.134781015C>T , CM000667.1:g.134781015C>T GRCh37
NC_000005.8:g.134808914C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000537858.2:c.*4129G>A (TIFAB) MANE Select ENSP00000440509.1:n.*4129G>A
ENST00000503143.3:c.*1049G>A (DCANP1) MANE Select ENSP00000421871.1:n.*1049G>A
ENST00000537858.1:c.*4129G>A (TIFAB) ENSP00000440509.1:n.*4129G>A
NM_130848.2:c.*1049G>A (DCANP1) NP_570900.1:n.*1049G>A
NM_001099221.2:c.*4129G>A (TIFAB) MANE Select NP_001092691.1:n.*4129G>A
NM_130848.3:c.*1049G>A (DCANP1) MANE Select NP_570900.1:n.*1049G>A
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