Canonical Allele Identifier: CA2241534820
Gene: CDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179551C= , CM000678.2:g.89179551C= GRCh38
NC_000016.9:g.89245959C= , CM000678.1:g.89245959C= GRCh37
NC_000016.8:g.87773460C= NCBI36
NG_012055.1:g.12797C=

Transcript Alleles

HGVS Amino-acid change
ENST00000289746.3:c.178C= MANE Select ENSP00000289746.2:p.Arg60=
ENST00000289746.2:c.178C= ENSP00000289746.2:p.Arg60=
ENST00000521087.5:n.243C=
ENST00000524089.1:n.243C=
NM_004933.2:c.178C= NP_004924.1:p.Arg60=
XM_011522806.1:c.178C= XP_011521108.1:p.Arg60=
NM_004933.3:c.178C= MANE Select NP_004924.1:p.Arg60=