Canonical Allele Identifier: CA359245178

Linked Data

gnomAD v4: 5-14713650-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14713650G>A , CM000667.2:g.14713650G>A GRCh38
NC_000005.9:g.14713759G>A , CM000667.1:g.14713759G>A GRCh37
NC_000005.8:g.14766759G>A NCBI36
NG_008273.1:g.163129C>T
NG_008273.2:g.163136C>T
NG_051625.1:g.57857G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1159C>T (ANKH) MANE Select ENSP00000284268.6:p.Leu387Phe
ENST00000284268.6:c.1159C>T (ANKH) ENSP00000284268.6:p.Leu387Phe
ENST00000502585.1:n.401C>T (ANKH)
NM_054027.4:c.1159C>T (ANKH) NP_473368.1:p.Leu387Phe
NR_046285.1:n.957G>A
NM_054027.5:c.1159C>T (ANKH) NP_473368.1:p.Leu387Phe
XM_011514151.2:c.*975G>A (OTULIN) XP_011512453.1:n.*975G>A
XM_017009644.2:c.1075C>T (ANKH) XP_016865133.1:p.Leu359Phe
NM_054027.6:c.1159C>T (ANKH) MANE Select NP_473368.1:p.Leu387Phe