Canonical Allele Identifier: CA355767123

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190126201A>G (hg19) ; chr3:g.190408412A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190408412A>G , CM000665.2:g.190408412A>G	GRCh38
NC_000003.11:g.190126201A>G , CM000665.1:g.190126201A>G	GRCh37
NC_000003.10:g.191608895A>G	NCBI36
NG_008149.1:g.25361A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.481A>G MANE Select	ENSP00000264734.3:p.Lys161Glu
ENST00000456423.2:c.115-1491A>G	ENSP00000414136.2:n.115-1491A>G
ENST00000264734.2:c.691A>G	ENSP00000264734.2:p.Lys231Glu
ENST00000456423.1:c.325-1491A>G	ENSP00000414136.1:n.325-1491A>G
NM_006580.3:c.691A>G	NP_006571.1:p.Lys231Glu
NM_001378492.1:c.481A>G	NP_001365421.1:p.Lys161Glu
NM_001378493.1:c.481A>G	NP_001365422.1:p.Lys161Glu
NM_006580.4:c.481A>G MANE Select	NP_006571.2:p.Lys161Glu