Canonical Allele Identifier: CA2830536168
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190405007_190405008insCACA , CM000665.2:g.190405007_190405008insCACA GRCh38
NC_000003.11:g.190122796_190122797insCACA , CM000665.1:g.190122796_190122797insCACA GRCh37
NC_000003.10:g.191605490_191605491insCACA NCBI36
NG_008149.1:g.21956_21957insCACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.382+81_382+82insCACA MANE Select ENSP00000264734.3:n.382+81_382+82insCACA
ENST00000456423.2:c.115-4896_115-4895insCACA ENSP00000414136.2:n.115-4896_115-4895insCACA
ENST00000264734.2:c.592+81_592+82insCACA ENSP00000264734.2:n.592+81_592+82insCACA
ENST00000456423.1:c.325-4896_325-4895insCACA ENSP00000414136.1:n.325-4896_325-4895insCACA
NM_006580.3:c.592+81_592+82insCACA NP_006571.1:n.592+81_592+82insCACA
NM_001378492.1:c.382+81_382+82insCACA NP_001365421.1:n.382+81_382+82insCACA
NM_001378493.1:c.382+81_382+82insCACA NP_001365422.1:n.382+81_382+82insCACA
NM_006580.4:c.382+81_382+82insCACA MANE Select NP_006571.2:n.382+81_382+82insCACA