Canonical Allele Identifier: CA2258420762
Gene: DUSP14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.37490515C= , CM000679.2:g.37490515C= GRCh38
NC_000017.10:g.35850621C= , CM000679.1:g.35850621C= GRCh37
NC_000017.9:g.32924734C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000617516.5:c.-181+557C= MANE Select ENSP00000478595.1:n.-181+557C=
ENST00000617516.4:c.-181+557C= ENSP00000478595.1:n.-181+557C=
NM_007026.3:c.-181+557C= NP_008957.1:n.-181+557C=
XM_011524234.1:c.-181+1560C= XP_011522536.1:n.-181+1560C=
XM_005256977.3:c.-1293C= XP_005257034.1:n.-1293C=
NM_007026.4:c.-181+557C= MANE Select NP_008957.1:n.-181+557C=