Canonical Allele Identifier: CA1428775826

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388282_190388285delinsAGGG , CM000665.2:g.190388282_190388285delinsAGGG	GRCh38
NC_000003.11:g.190106071_190106074delinsAGGG , CM000665.1:g.190106071_190106074delinsAGGG	GRCh37
NC_000003.10:g.191588765_191588768delinsAGGG	NCBI36
NG_008149.1:g.5231_5234delinsAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.-48_-45delinsAGGG MANE Select	ENSP00000264734.3:n.-48_-45delinsAGGG
ENST00000456423.2:c.-48_-45delinsAGGG	ENSP00000414136.2:n.-48_-45delinsAGGG
ENST00000264734.2:c.163_166delinsAGGG	ENSP00000264734.2:p.Arg55=
ENST00000456423.1:c.163_166delinsAGGG	ENSP00000414136.1:p.Arg55=
ENST00000468220.1:n.306+13679_306+13682delinsAGGG
NM_006580.3:c.163_166delinsAGGG	NP_006571.1:p.Arg55=
NM_001378492.1:c.-48_-45delinsAGGG	NP_001365421.1:n.-48_-45delinsAGGG
NM_001378493.1:c.-48_-45delinsAGGG	NP_001365422.1:n.-48_-45delinsAGGG
NM_006580.4:c.-48_-45delinsAGGG MANE Select	NP_006571.2:n.-48_-45delinsAGGG