Canonical Allele Identifier: CA1731904006
Community Standard Title: NC_000007.14:g.105902134T=
Gene: CDHR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.105902134T= , CM000669.2:g.105902134T= GRCh38
NC_000007.13:g.105542580T= , CM000669.1:g.105542580T= GRCh37
NC_000007.12:g.105329816T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000470188.5:n.438-8883T=
ENST00000487084.1:n.463-8093T=
ENST00000488386.5:c.-16+24877T= ENSP00000419593.1:n.-16+24877T=
XM_005250224.3:c.-16+24877T= XP_005250281.1:n.-16+24877T=
XM_005250224.5:c.-16+24877T= XP_005250281.1:n.-16+24877T=
XM_017011863.2:c.-403+24877T= XP_016867352.1:n.-403+24877T=
XM_017011865.2:c.-16+24877T= XP_016867354.1:n.-16+24877T=
XM_017011866.2:c.-506+24877T= XP_016867355.1:n.-506+24877T=
XM_017011867.2:c.-200+24877T= XP_016867356.1:n.-200+24877T=
XM_024446690.1:c.-303+24877T= XP_024302458.1:n.-303+24877T=