Canonical Allele Identifier: CA437418533
Gene: CLDN16 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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