Canonical Allele Identifier: CA2720991120
Gene: GATA3 HGNC NCBI

Linked Data

dbSNP Id: rs2131519683

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8073709_8073710insGT , CM000672.2:g.8073709_8073710insGT GRCh38
NC_000010.10:g.8115672_8115673insGT , CM000672.1:g.8115672_8115673insGT GRCh37
NC_000010.9:g.8155678_8155679insGT NCBI36
NG_015859.1:g.24006_24007insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000346208.4:c.1048-30_1048-29insGT ENSP00000341619.3:n.1048-30_1048-29insGT
ENST00000379328.9:c.1051-30_1051-29insGT MANE Select ENSP00000368632.3:n.1051-30_1051-29insGT
ENST00000346208.3:c.1048-30_1048-29insGT ENSP00000341619.3:n.1048-30_1048-29insGT
ENST00000379328.7:c.1051-30_1051-29insGT ENSP00000368632.3:n.1051-30_1051-29insGT
ENST00000461472.1:n.570-30_570-29insGT
NM_001002295.1:c.1051-30_1051-29insGT NP_001002295.1:n.1051-30_1051-29insGT
NM_002051.2:c.1048-30_1048-29insGT NP_002042.1:n.1048-30_1048-29insGT
XM_005252442.2:c.1051-30_1051-29insGT XP_005252499.1:n.1051-30_1051-29insGT
XM_005252443.3:c.1051-30_1051-29insGT XP_005252500.1:n.1051-30_1051-29insGT
XM_005252443.5:c.1051-30_1051-29insGT XP_005252500.1:n.1051-30_1051-29insGT
NM_001002295.2:c.1051-30_1051-29insGT MANE Select NP_001002295.1:n.1051-30_1051-29insGT
NM_002051.3:c.1048-30_1048-29insGT NP_002042.1:n.1048-30_1048-29insGT