Canonical Allele Identifier: CA397134811
Gene: CDH15 HGNC NCBI

Linked Data

dbSNP Id: rs1457609987
MyVariant Identifiers: chr16:g.89245876A>C (hg19) chr16:g.89179468A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179468A>C , CM000678.2:g.89179468A>C GRCh38
NC_000016.9:g.89245876A>C , CM000678.1:g.89245876A>C GRCh37
NC_000016.8:g.87773377A>C NCBI36
NG_012055.1:g.12714A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.95A>C MANE Select ENSP00000289746.2:p.Tyr32Ser
ENST00000289746.2:c.95A>C ENSP00000289746.2:p.Tyr32Ser
ENST00000521087.5:n.160A>C
ENST00000524089.1:n.160A>C
NM_004933.2:c.95A>C NP_004924.1:p.Tyr32Ser
XM_011522806.1:c.95A>C XP_011521108.1:p.Tyr32Ser
NM_004933.3:c.95A>C MANE Select NP_004924.1:p.Tyr32Ser
Search 100 bp 5'
Search 100 bp 3'