Canonical Allele Identifier: CA1057666639

Gene: CLDN16

Linked Data

• dbSNP Id: rs1718992316
• gnomAD v3: 3-190402588-A-C
• gnomAD v4: 3-190402588-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402588A>C , CM000665.2:g.190402588A>C	GRCh38
NC_000003.11:g.190120377A>C , CM000665.1:g.190120377A>C	GRCh37
NC_000003.10:g.191603071A>C	NCBI36
NG_008149.1:g.19537A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.217+149A>C MANE Select	ENSP00000264734.3:n.217+149A>C
ENST00000456423.2:c.115-7315A>C	ENSP00000414136.2:n.115-7315A>C
ENST00000264734.2:c.427+149A>C	ENSP00000264734.2:n.427+149A>C
ENST00000456423.1:c.325-7315A>C	ENSP00000414136.1:n.325-7315A>C
ENST00000468220.1:n.409+149A>C
NM_006580.3:c.427+149A>C	NP_006571.1:n.427+149A>C
NM_001378492.1:c.217+149A>C	NP_001365421.1:n.217+149A>C
NM_001378493.1:c.217+149A>C	NP_001365422.1:n.217+149A>C
NM_006580.4:c.217+149A>C MANE Select	NP_006571.2:n.217+149A>C