Canonical Allele Identifier: CA1428756826

Gene: CLDN16

Linked Data

• dbSNP Id: rs1718981214

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402272T>C , CM000665.2:g.190402272T>C	GRCh38
NC_000003.11:g.190120061T>C , CM000665.1:g.190120061T>C	GRCh37
NC_000003.10:g.191602755T>C	NCBI36
NG_008149.1:g.19221T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-65T>C MANE Select	ENSP00000264734.3:n.115-65T>C
ENST00000456423.2:c.115-7631T>C	ENSP00000414136.2:n.115-7631T>C
ENST00000264734.2:c.325-65T>C	ENSP00000264734.2:n.325-65T>C
ENST00000456423.1:c.325-7631T>C	ENSP00000414136.1:n.325-7631T>C
ENST00000468220.1:n.307-65T>C
NM_006580.3:c.325-65T>C	NP_006571.1:n.325-65T>C
NM_001378492.1:c.115-65T>C	NP_001365421.1:n.115-65T>C
NM_001378493.1:c.115-65T>C	NP_001365422.1:n.115-65T>C
NM_006580.4:c.115-65T>C MANE Select	NP_006571.2:n.115-65T>C