Canonical Allele Identifier: CA443295379

Linked Data

dbSNP Id: rs1371895000
gnomAD v2: 5-14713661-G-A
gnomAD v4: 5-14713552-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14713552G>A , CM000667.2:g.14713552G>A GRCh38
NC_000005.9:g.14713661G>A , CM000667.1:g.14713661G>A GRCh37
NC_000005.8:g.14766661G>A NCBI36
NG_008273.1:g.163227C>T
NG_008273.2:g.163234C>T
NG_051625.1:g.57759G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1257C>T (ANKH) MANE Select ENSP00000284268.6:p.Pro419=
ENST00000284268.6:c.1257C>T (ANKH) ENSP00000284268.6:p.Pro419=
ENST00000502585.1:n.499C>T (ANKH)
NM_054027.4:c.1257C>T (ANKH) NP_473368.1:p.Pro419=
NR_046285.1:n.859G>A
NM_054027.5:c.1257C>T (ANKH) NP_473368.1:p.Pro419=
XM_011514151.2:c.*877G>A (OTULIN) XP_011512453.1:n.*877G>A
XM_017009644.2:c.1173C>T (ANKH) XP_016865133.1:p.Pro391=
NM_054027.6:c.1257C>T (ANKH) MANE Select NP_473368.1:p.Pro419=