Canonical Allele Identifier: CA397134792
Gene: CDH15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.89245873T>A (hg19) chr16:g.89179465T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179465T>A , CM000678.2:g.89179465T>A GRCh38
NC_000016.9:g.89245873T>A , CM000678.1:g.89245873T>A GRCh37
NC_000016.8:g.87773374T>A NCBI36
NG_012055.1:g.12711T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.92T>A MANE Select ENSP00000289746.2:p.Leu31Gln
ENST00000289746.2:c.92T>A ENSP00000289746.2:p.Leu31Gln
ENST00000521087.5:n.157T>A
ENST00000524089.1:n.157T>A
NM_004933.2:c.92T>A NP_004924.1:p.Leu31Gln
XM_011522806.1:c.92T>A XP_011521108.1:p.Leu31Gln
NM_004933.3:c.92T>A MANE Select NP_004924.1:p.Leu31Gln
Search 100 bp 5'
Search 100 bp 3'