Canonical Allele Identifier: CA1660320179
Gene: TRDN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123218729_123218731delinsAAC , CM000668.2:g.123218729_123218731delinsAAC GRCh38
NC_000006.11:g.123539874_123539876delinsAAC , CM000668.1:g.123539874_123539876delinsAAC GRCh37
NC_000006.10:g.123581573_123581575delinsAAC NCBI36
NG_030438.1:g.423363_423365delinsGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.2060_2062delinsGTT MANE Select ENSP00000333984.5:p.Ser687=
ENST00000334268.8:c.2060_2062delinsGTT ENSP00000333984.5:p.Ser687=
NM_006073.3:c.2060_2062delinsGTT NP_006064.2:p.Ser687=
XM_011535382.1:c.1979_1981delinsGTT XP_011533684.1:p.Ser660=
NM_006073.4:c.2060_2062delinsGTT MANE Select NP_006064.2:p.Ser687=
Search 100 bp 5'
Search 100 bp 3'