Canonical Allele Identifier: CA1724999902

Gene: CLDN12

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.90413990C= , CM000669.2:g.90413990C=	GRCh38
NC_000007.13:g.90043304C= , CM000669.1:g.90043304C=	GRCh37
NC_000007.12:g.89881240C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001185072.3:c.*579C= MANE Select	NP_001172001.1:n.*579C=
ENST00000496677.6:c.*579C= MANE Select	ENSP00000419053.1:n.*579C=
NM_001185072.2:c.*579C=	NP_001172001.1:n.*579C=
NM_001185073.2:c.*579C=	NP_001172002.1:n.*579C=
NM_001185073.3:c.*579C=	NP_001172002.1:n.*579C=
NM_012129.4:c.*579C=	NP_036261.1:n.*579C=
NM_012129.5:c.*579C=	NP_036261.1:n.*579C=
ENST00000287916.8:c.*579C=	ENSP00000287916.4:n.*579C=
ENST00000394605.2:c.*579C=	ENSP00000378103.1:n.*579C=
ENST00000451941.6:n.32+8378C=
ENST00000483862.5:n.121+8382C=
ENST00000498033.5:n.156+8382C=
XR_002956513.1:n.723+4457G=
XR_927736.1:n.410+4457G=