Canonical Allele Identifier: CA350295826
Gene: TRAK2 HGNC NCBI
STRADB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201399465C>T , CM000664.2:g.201399465C>T GRCh38
NC_000002.11:g.202264188C>T , CM000664.1:g.202264188C>T GRCh37
NC_000002.10:g.201972433C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_015049.3:c.392G>A (TRAK2) MANE Select NP_055864.2:p.Arg131Gln
ENST00000332624.8:c.392G>A (TRAK2) MANE Select ENSP00000328875.3:p.Arg131Gln
NM_015049.2:c.392G>A (TRAK2) NP_055864.2:p.Arg131Gln
ENST00000332624.7:c.392G>A (TRAK2) ENSP00000328875.3:p.Arg131Gln
ENST00000430254.1:c.392G>A (TRAK2) ENSP00000409333.1:p.Arg131Gln
ENST00000458269.6:c.28+11390C>T (STRADB) ENSP00000409552.2:n.28+11390C>T
ENST00000486291.1:n.46G>A (TRAK2)
ENST00000620184.4:c.110G>A (TRAK2) ENSP00000482435.1:p.Arg37Gln
XM_006712714.1:c.-242G>A (TRAK2) XP_006712777.1:n.-242G>A
XM_011511690.1:c.392G>A (TRAK2) XP_011509992.1:p.Arg131Gln
XM_011511691.1:c.392G>A (TRAK2) XP_011509993.1:p.Arg131Gln
XM_017004772.1:c.-242G>A (TRAK2) XP_016860261.1:n.-242G>A