Canonical Allele Identifier: CA285373639

Linked Data

dbSNP Id: rs553989362

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83745371C>A , CM000678.2:g.83745371C>A GRCh38
NC_000016.9:g.83778976C>A , CM000678.1:g.83778976C>A GRCh37
NC_000016.8:g.82336477C>A NCBI36
NG_052819.1:g.1123578C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000690173.1:n.97+25964C>A (HSBP1)
ENST00000693379.1:n.97+25964C>A (HSBP1)
ENST00000693758.1:n.97+25964C>A (HSBP1)
ENST00000567109.6:c.1539-2737C>A (CDH13) MANE Select ENSP00000479395.1:n.1539-2737C>A
ENST00000268613.14:c.1680-2737C>A (CDH13) ENSP00000268613.10:n.1680-2737C>A
ENST00000428848.7:c.1422-2737C>A (CDH13) ENSP00000394557.3:n.1422-2737C>A
ENST00000539548.6:c.*1171-2737C>A (CDH13) ENSP00000442225.2:n.*1171-2737C>A
ENST00000566620.5:c.1503-2737C>A (CDH13) ENSP00000454435.3:n.1503-2737C>A
ENST00000567109.5:c.1539-2737C>A (CDH13) ENSP00000479395.1:n.1539-2737C>A
ENST00000615627.1:c.459-2737C>A (CDH13) ENSP00000482651.1:n.459-2737C>A
ENST00000622885.4:c.1383-2737C>A (CDH13) ENSP00000483719.1:n.1383-2737C>A
NM_001220488.1:c.1680-2737C>A (CDH13) NP_001207417.1:n.1680-2737C>A
NM_001220489.1:c.1422-2737C>A (CDH13) NP_001207418.1:n.1422-2737C>A
NM_001220490.1:c.777-2737C>A (CDH13) NP_001207419.1:n.777-2737C>A
NM_001257.4:c.1539-2737C>A (CDH13) NP_001248.1:n.1539-2737C>A
XM_011522804.1:c.1236-2737C>A (CDH13) XP_011521106.1:n.1236-2737C>A
XM_011522804.3:c.1236-2737C>A (CDH13) XP_011521106.1:n.1236-2737C>A
NM_001257.5:c.1539-2737C>A (CDH13) MANE Select NP_001248.1:n.1539-2737C>A
NM_001220488.2:c.1680-2737C>A (CDH13) NP_001207417.1:n.1680-2737C>A
NM_001220489.2:c.1422-2737C>A (CDH13) NP_001207418.1:n.1422-2737C>A
NM_001220490.2:c.777-2737C>A (CDH13) NP_001207419.1:n.777-2737C>A