Canonical Allele Identifier: CA530443777

Gene: TPO

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1413472A>T , CM000664.2:g.1413472A>T	GRCh38
NC_000002.11:g.1417244A>T , CM000664.1:g.1417244A>T	GRCh37
NC_000002.10:g.1396251A>T	NCBI36
NG_011581.1:g.5010A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329066.9:c.-75A>T MANE Select	ENSP00000329869.4:n.-75A>T
ENST00000329066.8:c.-75A>T	ENSP00000329869.4:n.-75A>T
ENST00000345913.8:c.-80A>T	ENSP00000318820.7:n.-80A>T
ENST00000382269.7:c.-75A>T	ENSP00000371704.3:n.-75A>T
ENST00000497517.6:n.180+39070A>T
ENST00000539820.5:c.-80A>T	ENSP00000444840.1:n.-80A>T
NM_000547.5:c.-80A>T	NP_000538.3:n.-80A>T
NM_001206744.1:c.-75A>T	NP_001193673.1:n.-75A>T
NM_001206745.1:c.-75A>T	NP_001193674.1:n.-75A>T
NM_175719.3:c.-80A>T	NP_783650.1:n.-80A>T
XM_024453087.1:c.-75A>T	XP_024308855.1:n.-75A>T
XM_024453088.1:c.-80A>T	XP_024308856.1:n.-80A>T
XM_024453089.1:c.-2+30A>T	XP_024308857.1:n.-2+30A>T
NM_001206744.2:c.-75A>T MANE Select	NP_001193673.1:n.-75A>T
NM_000547.6:c.-80A>T	NP_000538.3:n.-80A>T
NM_001206745.2:c.-75A>T	NP_001193674.1:n.-75A>T
NM_175719.4:c.-80A>T	NP_783650.1:n.-80A>T