Canonical Allele Identifier: CA2633641968

Gene: CDH5

Linked Data

• gnomAD v4: 16-66398428-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66398428T>C , CM000678.2:g.66398428T>C	GRCh38
NC_000016.9:g.66432331T>C , CM000678.1:g.66432331T>C	GRCh37
NC_000016.8:g.64989832T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000341529.8:c.1486-28T>C MANE Select	ENSP00000344115.3:n.1486-28T>C
ENST00000649567.1:c.1486-28T>C	ENSP00000497290.1:n.1486-28T>C
ENST00000341529.7:c.1486-28T>C	ENSP00000344115.3:n.1486-28T>C
ENST00000539168.1:c.-198-28T>C	ENSP00000461880.1:n.-198-28T>C
ENST00000565334.5:c.*609-28T>C	ENSP00000456028.1:n.*609-28T>C
ENST00000614547.4:c.1141-28T>C	ENSP00000479381.1:n.1141-28T>C
NM_001795.3:c.1486-28T>C	NP_001786.2:n.1486-28T>C
XM_011522801.1:c.1513-28T>C	XP_011521103.1:n.1513-28T>C
NM_001795.4:c.1486-28T>C	NP_001786.2:n.1486-28T>C
XM_011522801.2:c.1513-28T>C	XP_011521103.1:n.1513-28T>C
XM_024450133.1:c.1513-28T>C	XP_024305901.1:n.1513-28T>C
NM_001795.5:c.1486-28T>C MANE Select	NP_001786.2:n.1486-28T>C