Canonical Allele Identifier: CA2740617762

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716240G>T , CM000667.2:g.14716240G>T GRCh38
NC_000005.9:g.14716349G>T , CM000667.1:g.14716349G>T GRCh37
NC_000005.8:g.14769349G>T NCBI36
NG_008273.1:g.160539C>A
NG_008273.2:g.160546C>A
NG_051625.1:g.60447G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1141+466C>A (ANKH) MANE Select ENSP00000284268.6:n.1141+466C>A
ENST00000284268.6:c.1141+466C>A (ANKH) ENSP00000284268.6:n.1141+466C>A
ENST00000502585.1:n.383+466C>A (ANKH)
NM_054027.4:c.1141+466C>A (ANKH) NP_473368.1:n.1141+466C>A
NR_046285.1:n.2492-182G>T
NM_054027.5:c.1141+466C>A (ANKH) NP_473368.1:n.1141+466C>A
XM_011514151.2:c.*3565G>T (OTULIN) XP_011512453.1:n.*3565G>T
XM_017009644.2:c.1057+466C>A (ANKH) XP_016865133.1:n.1057+466C>A
NM_054027.6:c.1141+466C>A (ANKH) MANE Select NP_473368.1:n.1141+466C>A