Canonical Allele Identifier: CA649993993

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716262C>A , CM000667.2:g.14716262C>A GRCh38
NC_000005.9:g.14716371C>A , CM000667.1:g.14716371C>A GRCh37
NC_000005.8:g.14769371C>A NCBI36
NG_008273.1:g.160517G>T
NG_008273.2:g.160524G>T
NG_051625.1:g.60469C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1141+444G>T (ANKH) MANE Select ENSP00000284268.6:n.1141+444G>T
ENST00000284268.6:c.1141+444G>T (ANKH) ENSP00000284268.6:n.1141+444G>T
ENST00000502585.1:n.383+444G>T (ANKH)
NM_054027.4:c.1141+444G>T (ANKH) NP_473368.1:n.1141+444G>T
NR_046285.1:n.2492-160C>A
NM_054027.5:c.1141+444G>T (ANKH) NP_473368.1:n.1141+444G>T
XM_011514151.2:c.*3587C>A (OTULIN) XP_011512453.1:n.*3587C>A
XM_017009644.2:c.1057+444G>T (ANKH) XP_016865133.1:n.1057+444G>T
NM_054027.6:c.1141+444G>T (ANKH) MANE Select NP_473368.1:n.1141+444G>T