Canonical Allele Identifier: CA365564405
Gene: TRDN HGNC NCBI

Linked Data

gnomAD v4: 6-123218636-C-A
COSMIC: COSM5700547
MyVariant Identifiers: chr6:g.123539781C>A (hg19) chr6:g.123218636C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123218636C>A , CM000668.2:g.123218636C>A GRCh38
NC_000006.11:g.123539781C>A , CM000668.1:g.123539781C>A GRCh37
NC_000006.10:g.123581480C>A NCBI36
NG_030438.1:g.423458G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.2155G>T MANE Select ENSP00000333984.5:p.Ala719Ser
ENST00000334268.8:c.2155G>T ENSP00000333984.5:p.Ala719Ser
NM_006073.3:c.2155G>T NP_006064.2:p.Ala719Ser
XM_011535382.1:c.2074G>T XP_011533684.1:p.Ala692Ser
NM_006073.4:c.2155G>T MANE Select NP_006064.2:p.Ala719Ser
Search 100 bp 5'
Search 100 bp 3'