Canonical Allele Identifier: CA147262594
Gene: TRDN HGNC NCBI

Linked Data

dbSNP Id: rs873460

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123403337G>A , CM000668.2:g.123403337G>A GRCh38
NC_000006.11:g.123724482G>A , CM000668.1:g.123724482G>A GRCh37
NC_000006.10:g.123766181G>A NCBI36
NG_030438.1:g.238757C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.1052-9660C>T MANE Select ENSP00000333984.5:n.1052-9660C>T
ENST00000662930.1:c.1055-9660C>T ENSP00000499585.1:n.1055-9660C>T
ENST00000334268.8:c.1052-9660C>T ENSP00000333984.5:n.1052-9660C>T
NM_001251987.1:c.1055-9660C>T NP_001238916.1:n.1055-9660C>T
NM_006073.3:c.1052-9660C>T NP_006064.2:n.1052-9660C>T
XM_011535382.1:c.1052-9660C>T XP_011533684.1:n.1052-9660C>T
NM_006073.4:c.1052-9660C>T MANE Select NP_006064.2:n.1052-9660C>T
NM_001251987.2:c.1055-9660C>T NP_001238916.1:n.1055-9660C>T