Canonical Allele Identifier: CA355762104

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190388122-G-T
• MyVariant Identifiers: chr3:g.190105911G>T (hg19) ; chr3:g.190388122G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388122G>T , CM000665.2:g.190388122G>T	GRCh38
NC_000003.11:g.190105911G>T , CM000665.1:g.190105911G>T	GRCh37
NC_000003.10:g.191588605G>T	NCBI36
NG_008149.1:g.5071G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-208G>T	ENSP00000414136.2:n.-208G>T
ENST00000264734.2:c.3G>T	ENSP00000264734.2:p.Met1Ile
ENST00000456423.1:c.3G>T	ENSP00000414136.1:p.Met1Ile
ENST00000468220.1:n.306+13519G>T
NM_006580.3:c.3G>T	NP_006571.1:p.Met1Ile
NM_001378492.1:c.-93-115G>T	NP_001365421.1:n.-93-115G>T
NM_001378493.1:c.-93-115G>T	NP_001365422.1:n.-93-115G>T