Canonical Allele Identifier: CA924692074
Gene: GATA3 HGNC NCBI

Linked Data

dbSNP Id: rs1832967575

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8073708_8073709insCA , CM000672.2:g.8073708_8073709insCA GRCh38
NC_000010.10:g.8115671_8115672insCA , CM000672.1:g.8115671_8115672insCA GRCh37
NC_000010.9:g.8155677_8155678insCA NCBI36
NG_015859.1:g.24005_24006insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000346208.4:c.1048-31_1048-30insCA ENSP00000341619.3:n.1048-31_1048-30insCA
ENST00000379328.9:c.1051-31_1051-30insCA MANE Select ENSP00000368632.3:n.1051-31_1051-30insCA
ENST00000346208.3:c.1048-31_1048-30insCA ENSP00000341619.3:n.1048-31_1048-30insCA
ENST00000379328.7:c.1051-31_1051-30insCA ENSP00000368632.3:n.1051-31_1051-30insCA
ENST00000461472.1:n.570-31_570-30insCA
NM_001002295.1:c.1051-31_1051-30insCA NP_001002295.1:n.1051-31_1051-30insCA
NM_002051.2:c.1048-31_1048-30insCA NP_002042.1:n.1048-31_1048-30insCA
XM_005252442.2:c.1051-31_1051-30insCA XP_005252499.1:n.1051-31_1051-30insCA
XM_005252443.3:c.1051-31_1051-30insCA XP_005252500.1:n.1051-31_1051-30insCA
XM_005252443.5:c.1051-31_1051-30insCA XP_005252500.1:n.1051-31_1051-30insCA
NM_001002295.2:c.1051-31_1051-30insCA MANE Select NP_001002295.1:n.1051-31_1051-30insCA
NM_002051.3:c.1048-31_1048-30insCA NP_002042.1:n.1048-31_1048-30insCA