Canonical Allele Identifier: CA2373989122
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs2055064281
gnomAD v4: 20-61928079-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61928079G>A , CM000682.2:g.61928079G>A GRCh38
NC_000020.10:g.60503137G>A , CM000682.1:g.60503137G>A GRCh37
NC_000020.9:g.59936532G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.1772-111G>A MANE Select ENSP00000484928.1:n.1772-111G>A
ENST00000543233.2:c.1550-111G>A ENSP00000443301.1:n.1550-111G>A
ENST00000611855.4:c.1490-111G>A ENSP00000480844.1:n.1490-111G>A
ENST00000614565.4:c.1772-111G>A ENSP00000484928.1:n.1772-111G>A
NM_001252338.2:c.1661-111G>A NP_001239267.1:n.1661-111G>A
NM_001252339.2:c.1550-111G>A NP_001239268.1:n.1550-111G>A
NM_001794.4:c.1772-111G>A NP_001785.2:n.1772-111G>A
NM_001794.5:c.1772-111G>A MANE Select NP_001785.2:n.1772-111G>A
NM_001252339.3:c.1550-111G>A NP_001239268.1:n.1550-111G>A
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