Canonical Allele Identifier: CA2238191754

Gene: HSBP1 CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83745165_83745167delinsCTG , CM000678.2:g.83745165_83745167delinsCTG	GRCh38
NC_000016.9:g.83778770_83778772delinsCTG , CM000678.1:g.83778770_83778772delinsCTG	GRCh37
NC_000016.8:g.82336271_82336273delinsCTG	NCBI36
NG_052819.1:g.1123372_1123374delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690173.1:n.97+25758_97+25760delinsCTG (HSBP1)
ENST00000693379.1:n.97+25758_97+25760delinsCTG (HSBP1)
ENST00000693758.1:n.97+25758_97+25760delinsCTG (HSBP1)
ENST00000567109.6:c.1539-2943_1539-2941delinsCTG (CDH13) MANE Select	ENSP00000479395.1:n.1539-2943_1539-2941delinsCTG
ENST00000268613.14:c.1680-2943_1680-2941delinsCTG (CDH13)	ENSP00000268613.10:n.1680-2943_1680-2941delinsCTG
ENST00000428848.7:c.1422-2943_1422-2941delinsCTG (CDH13)	ENSP00000394557.3:n.1422-2943_1422-2941delinsCTG
ENST00000539548.6:c.*1171-2943_*1171-2941delinsCTG (CDH13)	ENSP00000442225.2:n.*1171-2943_*1171-2941delinsCTG
ENST00000566620.5:c.1503-2943_1503-2941delinsCTG (CDH13)	ENSP00000454435.3:n.1503-2943_1503-2941delinsCTG
ENST00000567109.5:c.1539-2943_1539-2941delinsCTG (CDH13)	ENSP00000479395.1:n.1539-2943_1539-2941delinsCTG
ENST00000615627.1:c.459-2943_459-2941delinsCTG (CDH13)	ENSP00000482651.1:n.459-2943_459-2941delinsCTG
ENST00000622885.4:c.1383-2943_1383-2941delinsCTG (CDH13)	ENSP00000483719.1:n.1383-2943_1383-2941delinsCTG
NM_001220488.1:c.1680-2943_1680-2941delinsCTG (CDH13)	NP_001207417.1:n.1680-2943_1680-2941delinsCTG
NM_001220489.1:c.1422-2943_1422-2941delinsCTG (CDH13)	NP_001207418.1:n.1422-2943_1422-2941delinsCTG
NM_001220490.1:c.777-2943_777-2941delinsCTG (CDH13)	NP_001207419.1:n.777-2943_777-2941delinsCTG
NM_001257.4:c.1539-2943_1539-2941delinsCTG (CDH13)	NP_001248.1:n.1539-2943_1539-2941delinsCTG
XM_011522804.1:c.1236-2943_1236-2941delinsCTG (CDH13)	XP_011521106.1:n.1236-2943_1236-2941delinsCTG
XM_011522804.3:c.1236-2943_1236-2941delinsCTG (CDH13)	XP_011521106.1:n.1236-2943_1236-2941delinsCTG
NM_001257.5:c.1539-2943_1539-2941delinsCTG (CDH13) MANE Select	NP_001248.1:n.1539-2943_1539-2941delinsCTG
NM_001220488.2:c.1680-2943_1680-2941delinsCTG (CDH13)	NP_001207417.1:n.1680-2943_1680-2941delinsCTG
NM_001220489.2:c.1422-2943_1422-2941delinsCTG (CDH13)	NP_001207418.1:n.1422-2943_1422-2941delinsCTG
NM_001220490.2:c.777-2943_777-2941delinsCTG (CDH13)	NP_001207419.1:n.777-2943_777-2941delinsCTG