Canonical Allele Identifier: CA636601573

Gene: CDH4

Linked Data

• dbSNP Id: rs1319920688
• gnomAD v2: 20-60106995-T-C
• gnomAD v3: 20-61531939-T-C
• gnomAD v4: 20-61531939-T-C
• MyVariant Identifiers: chr20:g.60106995T>C (hg19) ; chr20:g.61531939T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.61531939T>C , CM000682.2:g.61531939T>C	GRCh38
NC_000020.10:g.60106995T>C , CM000682.1:g.60106995T>C	GRCh37
NC_000020.9:g.59540390T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614565.5:c.170-211624T>C MANE Select	ENSP00000484928.1:n.170-211624T>C
ENST00000614565.4:c.170-211624T>C	ENSP00000484928.1:n.170-211624T>C
NM_001252338.2:c.58+32447T>C	NP_001239267.1:n.58+32447T>C
NM_001794.4:c.170-211624T>C	NP_001785.2:n.170-211624T>C
NM_001794.5:c.170-211624T>C MANE Select	NP_001785.2:n.170-211624T>C