Canonical Allele Identifier: CA2241534752
Gene: CDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179467T= , CM000678.2:g.89179467T= GRCh38
NC_000016.9:g.89245875T= , CM000678.1:g.89245875T= GRCh37
NC_000016.8:g.87773376T= NCBI36
NG_012055.1:g.12713T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.94T= MANE Select ENSP00000289746.2:p.Tyr32=
ENST00000289746.2:c.94T= ENSP00000289746.2:p.Tyr32=
ENST00000521087.5:n.159T=
ENST00000524089.1:n.159T=
NM_004933.2:c.94T= NP_004924.1:p.Tyr32=
XM_011522806.1:c.94T= XP_011521108.1:p.Tyr32=
NM_004933.3:c.94T= MANE Select NP_004924.1:p.Tyr32=