Canonical Allele Identifier: CA2765371408

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716280G>A , CM000667.2:g.14716280G>A GRCh38
NC_000005.9:g.14716389G>A , CM000667.1:g.14716389G>A GRCh37
NC_000005.8:g.14769389G>A NCBI36
NG_008273.1:g.160499C>T
NG_008273.2:g.160506C>T
NG_051625.1:g.60487G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1141+426C>T (ANKH) MANE Select ENSP00000284268.6:n.1141+426C>T
ENST00000284268.6:c.1141+426C>T (ANKH) ENSP00000284268.6:n.1141+426C>T
ENST00000502585.1:n.383+426C>T (ANKH)
NM_054027.4:c.1141+426C>T (ANKH) NP_473368.1:n.1141+426C>T
NR_046285.1:n.2492-142G>A
NM_054027.5:c.1141+426C>T (ANKH) NP_473368.1:n.1141+426C>T
XM_011514151.2:c.*3605G>A (OTULIN) XP_011512453.1:n.*3605G>A
XM_017009644.2:c.1057+426C>T (ANKH) XP_016865133.1:n.1057+426C>T
NM_054027.6:c.1141+426C>T (ANKH) MANE Select NP_473368.1:n.1141+426C>T