Canonical Allele Identifier: CA355766024
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190404797G>T , CM000665.2:g.190404797G>T GRCh38
NC_000003.11:g.190122586G>T , CM000665.1:g.190122586G>T GRCh37
NC_000003.10:g.191605280G>T NCBI36
NG_008149.1:g.21746G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.253G>T MANE Select ENSP00000264734.3:p.Ala85Ser
ENST00000456423.2:c.115-5106G>T ENSP00000414136.2:n.115-5106G>T
ENST00000264734.2:c.463G>T ENSP00000264734.2:p.Ala155Ser
ENST00000456423.1:c.325-5106G>T ENSP00000414136.1:n.325-5106G>T
ENST00000468220.1:n.445G>T
NM_006580.3:c.463G>T NP_006571.1:p.Ala155Ser
NM_001378492.1:c.253G>T NP_001365421.1:p.Ala85Ser
NM_001378493.1:c.253G>T NP_001365422.1:p.Ala85Ser
NM_006580.4:c.253G>T MANE Select NP_006571.2:p.Ala85Ser