Canonical Allele Identifier: CA2650334018
Gene: IRF6 HGNC NCBI

Linked Data

gnomAD v4: 1-209788414-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209788414T>C , CM000663.2:g.209788414T>C GRCh38
NC_000001.10:g.209961759T>C , CM000663.1:g.209961759T>C GRCh37
NC_000001.9:g.208028382T>C NCBI36
NG_007081.2:g.22721A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696133.1:c.1400+10A>G ENSP00000512426.1:n.1400+10A>G
ENST00000696134.1:c.*837A>G ENSP00000512427.1:n.*837A>G
ENST00000367021.8:c.*6A>G MANE Select ENSP00000355988.3:n.*6A>G
ENST00000643798.1:c.*920A>G ENSP00000496669.1:n.*920A>G
ENST00000367021.7:c.*6A>G ENSP00000355988.3:n.*6A>G
ENST00000542854.5:c.*6A>G ENSP00000440532.1:n.*6A>G
NM_001206696.1:c.*6A>G NP_001193625.1:n.*6A>G
NM_006147.3:c.*6A>G NP_006138.1:n.*6A>G
NM_006147.4:c.*6A>G MANE Select NP_006138.1:n.*6A>G
NM_001206696.2:c.*6A>G NP_001193625.1:n.*6A>G
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