Canonical Allele Identifier: CA2786559737
Gene: GATA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8073707_8073723dup , CM000672.2:g.8073707_8073723dup GRCh38
NC_000010.10:g.8115670_8115686dup , CM000672.1:g.8115670_8115686dup GRCh37
NC_000010.9:g.8155676_8155692dup NCBI36
NG_015859.1:g.24004_24020dup

Transcript Alleles

HGVS Amino-acid change
ENST00000346208.4:c.1048-32_1048-16dup ENSP00000341619.3:n.1048-32_1048-16dup
ENST00000379328.9:c.1051-32_1051-16dup MANE Select ENSP00000368632.3:n.1051-32_1051-16dup
ENST00000346208.3:c.1048-32_1048-16dup ENSP00000341619.3:n.1048-32_1048-16dup
ENST00000379328.7:c.1051-32_1051-16dup ENSP00000368632.3:n.1051-32_1051-16dup
ENST00000461472.1:n.570-32_570-16dup
NM_001002295.1:c.1051-32_1051-16dup NP_001002295.1:n.1051-32_1051-16dup
NM_002051.2:c.1048-32_1048-16dup NP_002042.1:n.1048-32_1048-16dup
XM_005252442.2:c.1051-32_1051-16dup XP_005252499.1:n.1051-32_1051-16dup
XM_005252443.3:c.1051-32_1051-16dup XP_005252500.1:n.1051-32_1051-16dup
XM_005252443.5:c.1051-32_1051-16dup XP_005252500.1:n.1051-32_1051-16dup
NM_001002295.2:c.1051-32_1051-16dup MANE Select NP_001002295.1:n.1051-32_1051-16dup
NM_002051.3:c.1048-32_1048-16dup NP_002042.1:n.1048-32_1048-16dup