Canonical Allele Identifier: CA2238182966

Gene: HSBP1 CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83730515_83730516delinsAC , CM000678.2:g.83730515_83730516delinsAC	GRCh38
NC_000016.9:g.83764120_83764121delinsAC , CM000678.1:g.83764120_83764121delinsAC	GRCh37
NC_000016.8:g.82321621_82321622delinsAC	NCBI36
NG_052819.1:g.1108722_1108723delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690173.1:n.97+11108_97+11109delinsAC (HSBP1)
ENST00000693379.1:n.97+11108_97+11109delinsAC (HSBP1)
ENST00000693758.1:n.97+11108_97+11109delinsAC (HSBP1)
ENST00000567109.6:c.1539-17593_1539-17592delinsAC (CDH13) MANE Select	ENSP00000479395.1:n.1539-17593_1539-17592delinsAC
ENST00000268613.14:c.1680-17593_1680-17592delinsAC (CDH13)	ENSP00000268613.10:n.1680-17593_1680-17592delinsAC
ENST00000428848.7:c.1422-17593_1422-17592delinsAC (CDH13)	ENSP00000394557.3:n.1422-17593_1422-17592delinsAC
ENST00000539548.6:c.*1171-17593_*1171-17592delinsAC (CDH13)	ENSP00000442225.2:n.*1171-17593_*1171-17592delinsAC
ENST00000566620.5:c.1503-17593_1503-17592delinsAC (CDH13)	ENSP00000454435.3:n.1503-17593_1503-17592delinsAC
ENST00000567109.5:c.1539-17593_1539-17592delinsAC (CDH13)	ENSP00000479395.1:n.1539-17593_1539-17592delinsAC
ENST00000615627.1:c.459-17593_459-17592delinsAC (CDH13)	ENSP00000482651.1:n.459-17593_459-17592delinsAC
ENST00000622885.4:c.1383-17593_1383-17592delinsAC (CDH13)	ENSP00000483719.1:n.1383-17593_1383-17592delinsAC
NM_001220488.1:c.1680-17593_1680-17592delinsAC (CDH13)	NP_001207417.1:n.1680-17593_1680-17592delinsAC
NM_001220489.1:c.1422-17593_1422-17592delinsAC (CDH13)	NP_001207418.1:n.1422-17593_1422-17592delinsAC
NM_001220490.1:c.777-17593_777-17592delinsAC (CDH13)	NP_001207419.1:n.777-17593_777-17592delinsAC
NM_001257.4:c.1539-17593_1539-17592delinsAC (CDH13)	NP_001248.1:n.1539-17593_1539-17592delinsAC
XM_011522804.1:c.1236-17593_1236-17592delinsAC (CDH13)	XP_011521106.1:n.1236-17593_1236-17592delinsAC
XM_011522804.3:c.1236-17593_1236-17592delinsAC (CDH13)	XP_011521106.1:n.1236-17593_1236-17592delinsAC
XR_001752382.2:n.409_410delinsGT
XR_933801.3:n.409_410delinsGT
NM_001257.5:c.1539-17593_1539-17592delinsAC (CDH13) MANE Select	NP_001248.1:n.1539-17593_1539-17592delinsAC
NM_001220488.2:c.1680-17593_1680-17592delinsAC (CDH13)	NP_001207417.1:n.1680-17593_1680-17592delinsAC
NM_001220489.2:c.1422-17593_1422-17592delinsAC (CDH13)	NP_001207418.1:n.1422-17593_1422-17592delinsAC
NM_001220490.2:c.777-17593_777-17592delinsAC (CDH13)	NP_001207419.1:n.777-17593_777-17592delinsAC