Canonical Allele Identifier: CA2608207626
Gene: GATA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8073718_8073723del , CM000672.2:g.8073718_8073723del GRCh38
NC_000010.10:g.8115681_8115686del , CM000672.1:g.8115681_8115686del GRCh37
NC_000010.9:g.8155687_8155692del NCBI36
NG_015859.1:g.24015_24020del

Transcript Alleles

HGVS Amino-acid Change
ENST00000346208.4:c.1048-21_1048-16del ENSP00000341619.3:n.1048-21_1048-16del
ENST00000379328.9:c.1051-21_1051-16del MANE Select ENSP00000368632.3:n.1051-21_1051-16del
ENST00000346208.3:c.1048-21_1048-16del ENSP00000341619.3:n.1048-21_1048-16del
ENST00000379328.7:c.1051-21_1051-16del ENSP00000368632.3:n.1051-21_1051-16del
ENST00000461472.1:n.570-21_570-16del
NM_001002295.1:c.1051-21_1051-16del NP_001002295.1:n.1051-21_1051-16del
NM_002051.2:c.1048-21_1048-16del NP_002042.1:n.1048-21_1048-16del
XM_005252442.2:c.1051-21_1051-16del XP_005252499.1:n.1051-21_1051-16del
XM_005252443.3:c.1051-21_1051-16del XP_005252500.1:n.1051-21_1051-16del
XM_005252443.5:c.1051-21_1051-16del XP_005252500.1:n.1051-21_1051-16del
NM_001002295.2:c.1051-21_1051-16del MANE Select NP_001002295.1:n.1051-21_1051-16del
NM_002051.3:c.1048-21_1048-16del NP_002042.1:n.1048-21_1048-16del