Canonical Allele Identifier: CA904289147

Gene: CLDN16

Linked Data

• dbSNP Id: rs1236412415
• MyVariant Identifiers: chr3:g.190122883A>T (hg19) ; chr3:g.190405094A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190405094A>T , CM000665.2:g.190405094A>T	GRCh38
NC_000003.11:g.190122883A>T , CM000665.1:g.190122883A>T	GRCh37
NC_000003.10:g.191605577A>T	NCBI36
NG_008149.1:g.22043A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.382+168A>T MANE Select	ENSP00000264734.3:n.382+168A>T
ENST00000456423.2:c.115-4809A>T	ENSP00000414136.2:n.115-4809A>T
ENST00000264734.2:c.592+168A>T	ENSP00000264734.2:n.592+168A>T
ENST00000456423.1:c.325-4809A>T	ENSP00000414136.1:n.325-4809A>T
NM_006580.3:c.592+168A>T	NP_006571.1:n.592+168A>T
NM_001378492.1:c.382+168A>T	NP_001365421.1:n.382+168A>T
NM_001378493.1:c.382+168A>T	NP_001365422.1:n.382+168A>T
NM_006580.4:c.382+168A>T MANE Select	NP_006571.2:n.382+168A>T