Canonical Allele Identifier: CA2258420737
Gene: DUSP14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.37490447C= , CM000679.2:g.37490447C= GRCh38
NC_000017.10:g.35850553C= , CM000679.1:g.35850553C= GRCh37
NC_000017.9:g.32924666C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000617516.5:c.-181+489C= MANE Select ENSP00000478595.1:n.-181+489C=
ENST00000617516.4:c.-181+489C= ENSP00000478595.1:n.-181+489C=
NM_007026.3:c.-181+489C= NP_008957.1:n.-181+489C=
XM_011524234.1:c.-181+1492C= XP_011522536.1:n.-181+1492C=
XM_005256977.3:c.-1361C= XP_005257034.1:n.-1361C=
NM_007026.4:c.-181+489C= MANE Select NP_008957.1:n.-181+489C=