Canonical Allele Identifier: CA1528877800

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14711166T= , CM000667.2:g.14711166T= GRCh38
NC_000005.9:g.14711275T= , CM000667.1:g.14711275T= GRCh37
NC_000005.8:g.14764275T= NCBI36
NG_008273.1:g.165613A=
NG_008273.2:g.165620A=
NG_051625.1:g.55373T=

Transcript Alleles

HGVS Amino-acid change
ENST00000284268.8:c.*31A= (ANKH) MANE Select ENSP00000284268.6:n.*31A=
ENST00000284268.6:c.*31A= (ANKH) ENSP00000284268.6:n.*31A=
ENST00000502585.1:n.752A= (ANKH)
NM_054027.4:c.*31A= (ANKH) NP_473368.1:n.*31A=
XM_011514151.1:c.*47-1556T= (OTULIN) XP_011512453.1:n.*47-1556T=
NM_054027.5:c.*31A= (ANKH) NP_473368.1:n.*31A=
XM_011514151.2:c.*47-1556T= (OTULIN) XP_011512453.1:n.*47-1556T=
XM_017009644.2:c.*31A= (ANKH) XP_016865133.1:n.*31A=
NM_054027.6:c.*31A= (ANKH) MANE Select NP_473368.1:n.*31A=