Canonical Allele Identifier: CA11286961
Gene: THADA HGNC NCBI

Linked Data

dbSNP Id: rs6732426
gnomAD v2: 2-43587504-C-T
gnomAD v3: 2-43360365-C-T
gnomAD v4: 2-43360365-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43360365C>T , CM000664.2:g.43360365C>T GRCh38
NC_000002.11:g.43587504C>T , CM000664.1:g.43587504C>T GRCh37
NC_000002.10:g.43441008C>T NCBI36
NG_051580.1:g.240682G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000405975.7:c.4228-16128G>A MANE Select ENSP00000386088.2:n.4228-16128G>A
ENST00000398653.5:c.*3144-16128G>A ENSP00000381647.1:n.*3144-16128G>A
ENST00000402796.5:c.2634-16128G>A ENSP00000385003.1:n.2634-16128G>A
ENST00000405006.8:c.4228-16128G>A ENSP00000385995.4:n.4228-16128G>A
ENST00000405975.6:c.4228-16128G>A ENSP00000386088.2:n.4228-16128G>A
ENST00000407351.5:c.1947-16128G>A
ENST00000408045.7:c.*3323-16128G>A ENSP00000384172.2:n.*3323-16128G>A
ENST00000473004.5:n.324+9755G>A
ENST00000485353.5:n.618-16128G>A
ENST00000486735.5:n.132-16128G>A
ENST00000497770.1:n.273+11600G>A
NM_001083953.1:c.4228-16128G>A NP_001077422.1:n.4228-16128G>A
NM_022065.4:c.4228-16128G>A NP_071348.3:n.4228-16128G>A
NR_073394.1:n.4178-16128G>A
XM_006712061.2:c.4228-16128G>A XP_006712124.1:n.4228-16128G>A
XM_006712062.1:c.4225-16128G>A XP_006712125.1:n.4225-16128G>A
XM_006712063.1:c.4108-16128G>A XP_006712126.1:n.4108-16128G>A
XM_006712064.1:c.4228-16128G>A XP_006712127.1:n.4228-16128G>A
XM_006712065.1:c.4006-16128G>A XP_006712128.1:n.4006-16128G>A
XM_006712066.1:c.3865-16128G>A XP_006712129.1:n.3865-16128G>A
XM_006712067.1:c.3862-16128G>A XP_006712130.1:n.3862-16128G>A
XM_006712068.2:c.4228-16128G>A XP_006712131.1:n.4228-16128G>A
XM_006712069.2:c.1777-16128G>A XP_006712132.1:n.1777-16128G>A
XM_011533016.1:c.1540-16128G>A XP_011531318.1:n.1540-16128G>A
NM_001345923.1:c.4225-16128G>A NP_001332852.1:n.4225-16128G>A
NM_001345924.1:c.4105-16128G>A NP_001332853.1:n.4105-16128G>A
NM_001345925.1:c.4228-16128G>A NP_001332854.1:n.4228-16128G>A
NR_144316.1:n.4367+37606G>A
XM_006712064.2:c.4228-16128G>A XP_006712127.1:n.4228-16128G>A
XM_006712068.3:c.4228-16128G>A XP_006712131.1:n.4228-16128G>A
XM_006712069.3:c.1777-16128G>A XP_006712132.1:n.1777-16128G>A
XM_017004675.1:c.1540-16128G>A XP_016860164.1:n.1540-16128G>A
NM_001083953.2:c.4228-16128G>A NP_001077422.1:n.4228-16128G>A
NM_001345923.2:c.4225-16128G>A NP_001332852.1:n.4225-16128G>A
NM_001345924.2:c.4105-16128G>A NP_001332853.1:n.4105-16128G>A
NM_001345925.2:c.4228-16128G>A NP_001332854.1:n.4228-16128G>A
NM_022065.5:c.4228-16128G>A MANE Select NP_071348.3:n.4228-16128G>A
NR_073394.2:n.4170-16128G>A
NR_144316.2:n.4359+37606G>A