Canonical Allele Identifier: CA1528880712
Gene: ANKH HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716600A= , CM000667.2:g.14716600A= GRCh38
NC_000005.9:g.14716709A= , CM000667.1:g.14716709A= GRCh37
NC_000005.8:g.14769709A= NCBI36
NG_008273.1:g.160179T=
NG_008273.2:g.160186T=
NG_051625.1:g.60807A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1141+106T= MANE Select ENSP00000284268.6:n.1141+106T=
ENST00000284268.6:c.1141+106T= ENSP00000284268.6:n.1141+106T=
ENST00000502585.1:n.383+106T=
NM_054027.4:c.1141+106T= NP_473368.1:n.1141+106T=
NM_054027.5:c.1141+106T= NP_473368.1:n.1141+106T=
XM_017009644.2:c.1057+106T= XP_016865133.1:n.1057+106T=
NM_054027.6:c.1141+106T= MANE Select NP_473368.1:n.1141+106T=
Search 100 bp 5'
Search 100 bp 3'