Canonical Allele Identifier: CA746282040
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs1371038101
gnomAD v3: 20-61531656-G-T
gnomAD v4: 20-61531656-G-T
MyVariant Identifiers: chr20:g.60106712G>T (hg19) chr20:g.61531656G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61531656G>T , CM000682.2:g.61531656G>T GRCh38
NC_000020.10:g.60106712G>T , CM000682.1:g.60106712G>T GRCh37
NC_000020.9:g.59540107G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.170-211907G>T MANE Select ENSP00000484928.1:n.170-211907G>T
ENST00000614565.4:c.170-211907G>T ENSP00000484928.1:n.170-211907G>T
NM_001252338.2:c.58+32164G>T NP_001239267.1:n.58+32164G>T
NM_001794.4:c.170-211907G>T NP_001785.2:n.170-211907G>T
NM_001794.5:c.170-211907G>T MANE Select NP_001785.2:n.170-211907G>T
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