Canonical Allele Identifier: CA1428759035
Gene: CLDN16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190404532C= , CM000665.2:g.190404532C= GRCh38
NC_000003.11:g.190122321C= , CM000665.1:g.190122321C= GRCh37
NC_000003.10:g.191605015C= NCBI36
NG_008149.1:g.21481C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.218-230C= MANE Select ENSP00000264734.3:n.218-230C=
ENST00000456423.2:c.115-5371C= ENSP00000414136.2:n.115-5371C=
ENST00000264734.2:c.428-230C= ENSP00000264734.2:n.428-230C=
ENST00000456423.1:c.325-5371C= ENSP00000414136.1:n.325-5371C=
ENST00000468220.1:n.410-230C=
NM_006580.3:c.428-230C= NP_006571.1:n.428-230C=
NM_001378492.1:c.218-230C= NP_001365421.1:n.218-230C=
NM_001378493.1:c.218-230C= NP_001365422.1:n.218-230C=
NM_006580.4:c.218-230C= MANE Select NP_006571.2:n.218-230C=
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