Canonical Allele Identifier: CA359245175

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14713649A>C , CM000667.2:g.14713649A>C GRCh38
NC_000005.9:g.14713758A>C , CM000667.1:g.14713758A>C GRCh37
NC_000005.8:g.14766758A>C NCBI36
NG_008273.1:g.163130T>G
NG_008273.2:g.163137T>G
NG_051625.1:g.57856A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1160T>G (ANKH) MANE Select ENSP00000284268.6:p.Leu387Arg
ENST00000284268.6:c.1160T>G (ANKH) ENSP00000284268.6:p.Leu387Arg
ENST00000502585.1:n.402T>G (ANKH)
NM_054027.4:c.1160T>G (ANKH) NP_473368.1:p.Leu387Arg
NR_046285.1:n.956A>C
NM_054027.5:c.1160T>G (ANKH) NP_473368.1:p.Leu387Arg
XM_011514151.2:c.*974A>C (OTULIN) XP_011512453.1:n.*974A>C
XM_017009644.2:c.1076T>G (ANKH) XP_016865133.1:p.Leu359Arg
NM_054027.6:c.1160T>G (ANKH) MANE Select NP_473368.1:p.Leu387Arg