Canonical Allele Identifier: CA2838503937
Gene: TAFA5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.48710766T>C , CM000684.2:g.48710766T>C GRCh38
NC_000022.10:g.49106578T>C , CM000684.1:g.49106578T>C GRCh37
NC_000022.9:g.47492584T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000402357.6:c.390+2922T>C MANE Select ENSP00000383933.2:n.390+2922T>C
ENST00000336769.9:c.390+2922T>C ENSP00000336812.5:n.390+2922T>C
ENST00000358295.9:c.369+2922T>C ENSP00000351043.5:n.369+2922T>C
ENST00000402357.5:c.390+2922T>C ENSP00000383933.1:n.390+2922T>C
ENST00000406880.1:c.153+2922T>C ENSP00000385603.1:n.153+2922T>C
ENST00000473898.1:n.247+2922T>C
NM_001082967.2:c.390+2922T>C NP_001076436.1:n.390+2922T>C
NM_015381.6:c.369+2922T>C NP_056196.2:n.369+2922T>C
NM_001082967.3:c.390+2922T>C MANE Select NP_001076436.1:n.390+2922T>C
NM_015381.7:c.369+2922T>C NP_056196.2:n.369+2922T>C
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