Canonical Allele Identifier: CA1888995871
Gene: GATA3 HGNC NCBI

Linked Data

dbSNP Id: rs1832965136

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8073601_8073604dup , CM000672.2:g.8073601_8073604dup GRCh38
NC_000010.10:g.8115564_8115567dup , CM000672.1:g.8115564_8115567dup GRCh37
NC_000010.9:g.8155570_8155573dup NCBI36
NG_015859.1:g.23898_23901dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000346208.4:c.1048-138_1048-135dup ENSP00000341619.3:n.1048-138_1048-135dup
ENST00000379328.9:c.1051-138_1051-135dup MANE Select ENSP00000368632.3:n.1051-138_1051-135dup
ENST00000346208.3:c.1048-138_1048-135dup ENSP00000341619.3:n.1048-138_1048-135dup
ENST00000379328.7:c.1051-138_1051-135dup ENSP00000368632.3:n.1051-138_1051-135dup
ENST00000461472.1:n.570-138_570-135dup
NM_001002295.1:c.1051-138_1051-135dup NP_001002295.1:n.1051-138_1051-135dup
NM_002051.2:c.1048-138_1048-135dup NP_002042.1:n.1048-138_1048-135dup
XM_005252442.2:c.1051-138_1051-135dup XP_005252499.1:n.1051-138_1051-135dup
XM_005252443.3:c.1051-138_1051-135dup XP_005252500.1:n.1051-138_1051-135dup
XM_005252443.5:c.1051-138_1051-135dup XP_005252500.1:n.1051-138_1051-135dup
NM_001002295.2:c.1051-138_1051-135dup MANE Select NP_001002295.1:n.1051-138_1051-135dup
NM_002051.3:c.1048-138_1048-135dup NP_002042.1:n.1048-138_1048-135dup