Canonical Allele Identifier: CA359245191

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14713655G>T , CM000667.2:g.14713655G>T GRCh38
NC_000005.9:g.14713764G>T , CM000667.1:g.14713764G>T GRCh37
NC_000005.8:g.14766764G>T NCBI36
NG_008273.1:g.163124C>A
NG_008273.2:g.163131C>A
NG_051625.1:g.57862G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1154C>A (ANKH) MANE Select ENSP00000284268.6:p.Ala385Glu
ENST00000284268.6:c.1154C>A (ANKH) ENSP00000284268.6:p.Ala385Glu
ENST00000502585.1:n.396C>A (ANKH)
NM_054027.4:c.1154C>A (ANKH) NP_473368.1:p.Ala385Glu
NR_046285.1:n.962G>T
NM_054027.5:c.1154C>A (ANKH) NP_473368.1:p.Ala385Glu
XM_011514151.2:c.*980G>T (OTULIN) XP_011512453.1:n.*980G>T
XM_017009644.2:c.1070C>A (ANKH) XP_016865133.1:p.Ala357Glu
NM_054027.6:c.1154C>A (ANKH) MANE Select NP_473368.1:p.Ala385Glu