Canonical Allele Identifier: CA2669041508
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190404690_190404691dup , CM000665.2:g.190404690_190404691dup GRCh38
NC_000003.11:g.190122479_190122480dup , CM000665.1:g.190122479_190122480dup GRCh37
NC_000003.10:g.191605173_191605174dup NCBI36
NG_008149.1:g.21639_21640dup

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.218-72_218-71dup MANE Select ENSP00000264734.3:n.218-72_218-71dup
ENST00000456423.2:c.115-5213_115-5212dup ENSP00000414136.2:n.115-5213_115-5212dup
ENST00000264734.2:c.428-72_428-71dup ENSP00000264734.2:n.428-72_428-71dup
ENST00000456423.1:c.325-5213_325-5212dup ENSP00000414136.1:n.325-5213_325-5212dup
ENST00000468220.1:n.410-72_410-71dup
NM_006580.3:c.428-72_428-71dup NP_006571.1:n.428-72_428-71dup
NM_001378492.1:c.218-72_218-71dup NP_001365421.1:n.218-72_218-71dup
NM_001378493.1:c.218-72_218-71dup NP_001365422.1:n.218-72_218-71dup
NM_006580.4:c.218-72_218-71dup MANE Select NP_006571.2:n.218-72_218-71dup