Canonical Allele Identifier: CA1428762775

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190408408A= , CM000665.2:g.190408408A=	GRCh38
NC_000003.11:g.190126197A= , CM000665.1:g.190126197A=	GRCh37
NC_000003.10:g.191608891A=	NCBI36
NG_008149.1:g.25357A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.477A= MANE Select	ENSP00000264734.3:p.Gln159=
ENST00000456423.2:c.115-1495A=	ENSP00000414136.2:n.115-1495A=
ENST00000264734.2:c.687A=	ENSP00000264734.2:p.Gln229=
ENST00000456423.1:c.325-1495A=	ENSP00000414136.1:n.325-1495A=
NM_006580.3:c.687A=	NP_006571.1:p.Gln229=
NM_001378492.1:c.477A=	NP_001365421.1:p.Gln159=
NM_001378493.1:c.477A=	NP_001365422.1:p.Gln159=
NM_006580.4:c.477A= MANE Select	NP_006571.2:p.Gln159=