Canonical Allele Identifier: CA437418535
Gene: CLDN16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.190126113A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408324A>T , CM000665.2:g.190408324A>T GRCh38
NC_000003.11:g.190126113A>T , CM000665.1:g.190126113A>T GRCh37
NC_000003.10:g.191608807A>T NCBI36
NG_008149.1:g.25273A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.393A>T MANE Select ENSP00000264734.3:p.Gly131=
ENST00000456423.2:c.115-1579A>T ENSP00000414136.2:n.115-1579A>T
ENST00000264734.2:c.603A>T ENSP00000264734.2:p.Gly201=
ENST00000456423.1:c.325-1579A>T ENSP00000414136.1:n.325-1579A>T
NM_006580.3:c.603A>T NP_006571.1:p.Gly201=
NM_001378492.1:c.393A>T NP_001365421.1:p.Gly131=
NM_001378493.1:c.393A>T NP_001365422.1:p.Gly131=
NM_006580.4:c.393A>T MANE Select NP_006571.2:p.Gly131=