Canonical Allele Identifier: CA1528879232

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14713653G= , CM000667.2:g.14713653G= GRCh38
NC_000005.9:g.14713762G= , CM000667.1:g.14713762G= GRCh37
NC_000005.8:g.14766762G= NCBI36
NG_008273.1:g.163126C=
NG_008273.2:g.163133C=
NG_051625.1:g.57860G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1156C= (ANKH) MANE Select ENSP00000284268.6:p.His386=
ENST00000284268.6:c.1156C= (ANKH) ENSP00000284268.6:p.His386=
ENST00000502585.1:n.398C= (ANKH)
NM_054027.4:c.1156C= (ANKH) NP_473368.1:p.His386=
NR_046285.1:n.960G=
NM_054027.5:c.1156C= (ANKH) NP_473368.1:p.His386=
XM_011514151.2:c.*978G= (OTULIN) XP_011512453.1:n.*978G=
XM_017009644.2:c.1072C= (ANKH) XP_016865133.1:p.His358=
NM_054027.6:c.1156C= (ANKH) MANE Select NP_473368.1:p.His386=