Canonical Allele Identifier: CA46914550
Gene: THADA HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs13429458

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43411699A>C , CM000664.2:g.43411699A>C GRCh38
NC_000002.10:g.43492342A>C NCBI36
NC_000002.11:g.43638838A>C , CM000664.1:g.43638838A>C GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000398653.5:c.*2975-13560T>G ENSP00000381647.1:p.=
ENST00000402796.5:n.2465-13560T>G ENSP00000385003.1:p.=
ENST00000405006.8:c.4059-13560T>G ENSP00000385995.4:p.=
ENST00000405975.6:c.4059-13560T>G ENSP00000386088.2:p.=
ENST00000407351.5:n.1778-13560T>G
ENST00000408045.7:c.*3154-13560T>G ENSP00000384172.2:p.=
ENST00000485353.5:n.449-13560T>G
NM_001083953.1:c.4059-13560T>G VV NP_001077422.1:p.=
NM_022065.4:c.4059-13560T>G VV NP_071348.3:p.=
NR_073394.1:n.4009-13560T>G
XM_006712061.2:c.4059-13560T>G XP_006712124.1:p.=
XM_006712062.1:c.4056-13560T>G XP_006712125.1:p.=
XM_006712063.1:c.3939-13560T>G XP_006712126.1:p.=
XM_006712064.1:c.4059-13560T>G XP_006712127.1:p.=
XM_006712065.1:c.3837-13560T>G XP_006712128.1:p.=
XM_006712066.1:c.3696-13560T>G XP_006712129.1:p.=
XM_006712067.1:c.3693-13560T>G XP_006712130.1:p.=
XM_006712068.2:c.4059-13560T>G XP_006712131.1:p.=
XM_006712069.2:c.1608-13560T>G XP_006712132.1:p.=
XM_011533016.1:c.1371-13560T>G XP_011531318.1:p.=