Canonical Allele Identifier: CA285365818

Gene: HSBP1 CDH13

Linked Data

• dbSNP Id: rs928733185
• gnomAD v3: 16-83737956-A-G
• gnomAD v4: 16-83737956-A-G
• MyVariant Identifiers: chr16:g.83771561A>G (hg19) ; chr16:g.83737956A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83737956A>G , CM000678.2:g.83737956A>G	GRCh38
NC_000016.9:g.83771561A>G , CM000678.1:g.83771561A>G	GRCh37
NC_000016.8:g.82329062A>G	NCBI36
NG_052819.1:g.1116163A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690173.1:n.97+18549A>G (HSBP1)
ENST00000693379.1:n.97+18549A>G (HSBP1)
ENST00000693758.1:n.97+18549A>G (HSBP1)
ENST00000567109.6:c.1539-10152A>G (CDH13) MANE Select	ENSP00000479395.1:n.1539-10152A>G
ENST00000268613.14:c.1680-10152A>G (CDH13)	ENSP00000268613.10:n.1680-10152A>G
ENST00000428848.7:c.1422-10152A>G (CDH13)	ENSP00000394557.3:n.1422-10152A>G
ENST00000539548.6:c.*1171-10152A>G (CDH13)	ENSP00000442225.2:n.*1171-10152A>G
ENST00000566620.5:c.1503-10152A>G (CDH13)	ENSP00000454435.3:n.1503-10152A>G
ENST00000567109.5:c.1539-10152A>G (CDH13)	ENSP00000479395.1:n.1539-10152A>G
ENST00000615627.1:c.459-10152A>G (CDH13)	ENSP00000482651.1:n.459-10152A>G
ENST00000622885.4:c.1383-10152A>G (CDH13)	ENSP00000483719.1:n.1383-10152A>G
NM_001220488.1:c.1680-10152A>G (CDH13)	NP_001207417.1:n.1680-10152A>G
NM_001220489.1:c.1422-10152A>G (CDH13)	NP_001207418.1:n.1422-10152A>G
NM_001220490.1:c.777-10152A>G (CDH13)	NP_001207419.1:n.777-10152A>G
NM_001257.4:c.1539-10152A>G (CDH13)	NP_001248.1:n.1539-10152A>G
XM_011522804.1:c.1236-10152A>G (CDH13)	XP_011521106.1:n.1236-10152A>G
XM_011522804.3:c.1236-10152A>G (CDH13)	XP_011521106.1:n.1236-10152A>G
NM_001257.5:c.1539-10152A>G (CDH13) MANE Select	NP_001248.1:n.1539-10152A>G
NM_001220488.2:c.1680-10152A>G (CDH13)	NP_001207417.1:n.1680-10152A>G
NM_001220489.2:c.1422-10152A>G (CDH13)	NP_001207418.1:n.1422-10152A>G
NM_001220490.2:c.777-10152A>G (CDH13)	NP_001207419.1:n.777-10152A>G