Canonical Allele Identifier: CA2238194863

Gene: HSBP1 CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83750323T= , CM000678.2:g.83750323T=	GRCh38
NC_000016.9:g.83783928T= , CM000678.1:g.83783928T=	GRCh37
NC_000016.8:g.82341429T=	NCBI36
NG_052819.1:g.1128530T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690173.1:n.97+30916T= (HSBP1)
ENST00000693379.1:n.97+30916T= (HSBP1)
ENST00000693758.1:n.97+30916T= (HSBP1)
ENST00000567109.6:c.1681+2073T= (CDH13) MANE Select	ENSP00000479395.1:n.1681+2073T=
ENST00000268613.14:c.1822+2073T= (CDH13)	ENSP00000268613.10:n.1822+2073T=
ENST00000428848.7:c.1564+2073T= (CDH13)	ENSP00000394557.3:n.1564+2073T=
ENST00000539548.6:c.*1313+2073T= (CDH13)	ENSP00000442225.2:n.*1313+2073T=
ENST00000566620.5:c.1645+2073T= (CDH13)	ENSP00000454435.3:n.1645+2073T=
ENST00000567109.5:c.1681+2073T= (CDH13)	ENSP00000479395.1:n.1681+2073T=
ENST00000615627.1:c.601+2073T= (CDH13)	ENSP00000482651.1:n.601+2073T=
ENST00000622885.4:c.1525+2073T= (CDH13)	ENSP00000483719.1:n.1525+2073T=
NM_001220488.1:c.1822+2073T= (CDH13)	NP_001207417.1:n.1822+2073T=
NM_001220489.1:c.1564+2073T= (CDH13)	NP_001207418.1:n.1564+2073T=
NM_001220490.1:c.919+2073T= (CDH13)	NP_001207419.1:n.919+2073T=
NM_001257.4:c.1681+2073T= (CDH13)	NP_001248.1:n.1681+2073T=
XM_011522804.1:c.1378+2073T= (CDH13)	XP_011521106.1:n.1378+2073T=
XM_011522804.3:c.1378+2073T= (CDH13)	XP_011521106.1:n.1378+2073T=
NM_001257.5:c.1681+2073T= (CDH13) MANE Select	NP_001248.1:n.1681+2073T=
NM_001220488.2:c.1822+2073T= (CDH13)	NP_001207417.1:n.1822+2073T=
NM_001220489.2:c.1564+2073T= (CDH13)	NP_001207418.1:n.1564+2073T=
NM_001220490.2:c.919+2073T= (CDH13)	NP_001207419.1:n.919+2073T=