Canonical Allele Identifier: CA89760894

Gene: CLDN16

Linked Data

• dbSNP Id: rs990356250
• gnomAD v2: 3-190119894-C-T
• gnomAD v3: 3-190402105-C-T
• gnomAD v4: 3-190402105-C-T
• MyVariant Identifiers: chr3:g.190119894C>T (hg19) ; chr3:g.190402105C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402105C>T , CM000665.2:g.190402105C>T	GRCh38
NC_000003.11:g.190119894C>T , CM000665.1:g.190119894C>T	GRCh37
NC_000003.10:g.191602588C>T	NCBI36
NG_008149.1:g.19054C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-232C>T MANE Select	ENSP00000264734.3:n.115-232C>T
ENST00000456423.2:c.115-7798C>T	ENSP00000414136.2:n.115-7798C>T
ENST00000264734.2:c.325-232C>T	ENSP00000264734.2:n.325-232C>T
ENST00000456423.1:c.325-7798C>T	ENSP00000414136.1:n.325-7798C>T
ENST00000468220.1:n.307-232C>T
NM_006580.3:c.325-232C>T	NP_006571.1:n.325-232C>T
NM_001378492.1:c.115-232C>T	NP_001365421.1:n.115-232C>T
NM_001378493.1:c.115-232C>T	NP_001365422.1:n.115-232C>T
NM_006580.4:c.115-232C>T MANE Select	NP_006571.2:n.115-232C>T