Canonical Allele Identifier: CA1528879228

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14713644C= , CM000667.2:g.14713644C= GRCh38
NC_000005.9:g.14713753C= , CM000667.1:g.14713753C= GRCh37
NC_000005.8:g.14766753C= NCBI36
NG_008273.1:g.163135G=
NG_008273.2:g.163142G=
NG_051625.1:g.57851C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1165G= (ANKH) MANE Select ENSP00000284268.6:p.Gly389=
ENST00000284268.6:c.1165G= (ANKH) ENSP00000284268.6:p.Gly389=
ENST00000502585.1:n.407G= (ANKH)
NM_054027.4:c.1165G= (ANKH) NP_473368.1:p.Gly389=
NR_046285.1:n.951C=
NM_054027.5:c.1165G= (ANKH) NP_473368.1:p.Gly389=
XM_011514151.2:c.*969C= (OTULIN) XP_011512453.1:n.*969C=
XM_017009644.2:c.1081G= (ANKH) XP_016865133.1:p.Gly361=
NM_054027.6:c.1165G= (ANKH) MANE Select NP_473368.1:p.Gly389=