Canonical Allele Identifier: CA3983577
Community Standard Title: NM_006073.4(TRDN):c.2187G>T (p.Gln729His)
Gene: TRDN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123218604C>A , CM000668.2:g.123218604C>A GRCh38
NC_000006.11:g.123539749C>A , CM000668.1:g.123539749C>A GRCh37
NC_000006.10:g.123581448C>A NCBI36
NG_030438.1:g.423490G>T

Transcript Alleles

HGVS Amino-acid Change
NM_006073.4:c.2187G>T MANE Select NP_006064.2:p.Gln729His
ENST00000334268.9:c.2187G>T MANE Select ENSP00000333984.5:p.Gln729His
NM_006073.3:c.2187G>T NP_006064.2:p.Gln729His
ENST00000334268.8:c.2187G>T ENSP00000333984.5:p.Gln729His
XM_011535382.1:c.2106G>T XP_011533684.1:p.Gln702His