Canonical Allele Identifier: CA359244986

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14713557G>C , CM000667.2:g.14713557G>C GRCh38
NC_000005.9:g.14713666G>C , CM000667.1:g.14713666G>C GRCh37
NC_000005.8:g.14766666G>C NCBI36
NG_008273.1:g.163222C>G
NG_008273.2:g.163229C>G
NG_051625.1:g.57764G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1252C>G (ANKH) MANE Select ENSP00000284268.6:p.Leu418Val
ENST00000284268.6:c.1252C>G (ANKH) ENSP00000284268.6:p.Leu418Val
ENST00000502585.1:n.494C>G (ANKH)
NM_054027.4:c.1252C>G (ANKH) NP_473368.1:p.Leu418Val
NR_046285.1:n.864G>C
NM_054027.5:c.1252C>G (ANKH) NP_473368.1:p.Leu418Val
XM_011514151.2:c.*882G>C (OTULIN) XP_011512453.1:n.*882G>C
XM_017009644.2:c.1168C>G (ANKH) XP_016865133.1:p.Leu390Val
NM_054027.6:c.1252C>G (ANKH) MANE Select NP_473368.1:p.Leu418Val