Canonical Allele Identifier: CA2708135752

Linked Data

dbSNP Id: rs2126413587

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716232T>C , CM000667.2:g.14716232T>C GRCh38
NC_000005.9:g.14716341T>C , CM000667.1:g.14716341T>C GRCh37
NC_000005.8:g.14769341T>C NCBI36
NG_008273.1:g.160547A>G
NG_008273.2:g.160554A>G
NG_051625.1:g.60439T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1141+474A>G (ANKH) MANE Select ENSP00000284268.6:n.1141+474A>G
ENST00000284268.6:c.1141+474A>G (ANKH) ENSP00000284268.6:n.1141+474A>G
ENST00000502585.1:n.383+474A>G (ANKH)
NM_054027.4:c.1141+474A>G (ANKH) NP_473368.1:n.1141+474A>G
NR_046285.1:n.2492-190T>C
NM_054027.5:c.1141+474A>G (ANKH) NP_473368.1:n.1141+474A>G
XM_011514151.2:c.*3557T>C (OTULIN) XP_011512453.1:n.*3557T>C
XM_017009644.2:c.1057+474A>G (ANKH) XP_016865133.1:n.1057+474A>G
NM_054027.6:c.1141+474A>G (ANKH) MANE Select NP_473368.1:n.1141+474A>G