Canonical Allele Identifier: CA2241534791
Gene: CDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179532C= , CM000678.2:g.89179532C= GRCh38
NC_000016.9:g.89245940C= , CM000678.1:g.89245940C= GRCh37
NC_000016.8:g.87773441C= NCBI36
NG_012055.1:g.12778C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.159C= MANE Select ENSP00000289746.2:p.Ser53=
ENST00000289746.2:c.159C= ENSP00000289746.2:p.Ser53=
ENST00000521087.5:n.224C=
ENST00000524089.1:n.224C=
NM_004933.2:c.159C= NP_004924.1:p.Ser53=
XM_011522806.1:c.159C= XP_011521108.1:p.Ser53=
NM_004933.3:c.159C= MANE Select NP_004924.1:p.Ser53=