Canonical Allele Identifier: CA397135139
Gene: CDH15 HGNC NCBI

Linked Data

dbSNP Id: rs1398397019
gnomAD v4: 16-89179524-C-T
MyVariant Identifiers: chr16:g.89245932C>T (hg19) chr16:g.89179524C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179524C>T , CM000678.2:g.89179524C>T GRCh38
NC_000016.9:g.89245932C>T , CM000678.1:g.89245932C>T GRCh37
NC_000016.8:g.87773433C>T NCBI36
NG_012055.1:g.12770C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.151C>T MANE Select ENSP00000289746.2:p.Pro51Ser
ENST00000289746.2:c.151C>T ENSP00000289746.2:p.Pro51Ser
ENST00000521087.5:n.216C>T
ENST00000524089.1:n.216C>T
NM_004933.2:c.151C>T NP_004924.1:p.Pro51Ser
XM_011522806.1:c.151C>T XP_011521108.1:p.Pro51Ser
NM_004933.3:c.151C>T MANE Select NP_004924.1:p.Pro51Ser
Search 100 bp 5'
Search 100 bp 3'