Canonical Allele Identifier: CA904287639

Gene: CLDN16

Linked Data

• dbSNP Id: rs1197329709
• gnomAD v3: 3-190402669-A-T
• gnomAD v4: 3-190402669-A-T
• MyVariant Identifiers: chr3:g.190120458A>T (hg19) ; chr3:g.190402669A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402669A>T , CM000665.2:g.190402669A>T	GRCh38
NC_000003.11:g.190120458A>T , CM000665.1:g.190120458A>T	GRCh37
NC_000003.10:g.191603152A>T	NCBI36
NG_008149.1:g.19618A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.217+230A>T MANE Select	ENSP00000264734.3:n.217+230A>T
ENST00000456423.2:c.115-7234A>T	ENSP00000414136.2:n.115-7234A>T
ENST00000264734.2:c.427+230A>T	ENSP00000264734.2:n.427+230A>T
ENST00000456423.1:c.325-7234A>T	ENSP00000414136.1:n.325-7234A>T
ENST00000468220.1:n.409+230A>T
NM_006580.3:c.427+230A>T	NP_006571.1:n.427+230A>T
NM_001378492.1:c.217+230A>T	NP_001365421.1:n.217+230A>T
NM_001378493.1:c.217+230A>T	NP_001365422.1:n.217+230A>T
NM_006580.4:c.217+230A>T MANE Select	NP_006571.2:n.217+230A>T