Canonical Allele Identifier: CA648077544

Gene: CLDN16

Linked Data

• COSMIC: COSN9541116

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190405100G>C , CM000665.2:g.190405100G>C	GRCh38
NC_000003.11:g.190122889G>C , CM000665.1:g.190122889G>C	GRCh37
NC_000003.10:g.191605583G>C	NCBI36
NG_008149.1:g.22049G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.382+174G>C MANE Select	ENSP00000264734.3:n.382+174G>C
ENST00000456423.2:c.115-4803G>C	ENSP00000414136.2:n.115-4803G>C
ENST00000264734.2:c.592+174G>C	ENSP00000264734.2:n.592+174G>C
ENST00000456423.1:c.325-4803G>C	ENSP00000414136.1:n.325-4803G>C
NM_006580.3:c.592+174G>C	NP_006571.1:n.592+174G>C
NM_001378492.1:c.382+174G>C	NP_001365421.1:n.382+174G>C
NM_001378493.1:c.382+174G>C	NP_001365422.1:n.382+174G>C
NM_006580.4:c.382+174G>C MANE Select	NP_006571.2:n.382+174G>C