Canonical Allele Identifier: CA2786559741
Gene: GATA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8073883_8073884insAACACACCC , CM000672.2:g.8073883_8073884insAACACACCC GRCh38
NC_000010.10:g.8115846_8115847insAACACACCC , CM000672.1:g.8115846_8115847insAACACACCC GRCh37
NC_000010.9:g.8155852_8155853insAACACACCC NCBI36
NG_015859.1:g.24180_24181insAACACACCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000346208.4:c.1192_1193insAACACACCC ENSP00000341619.3:p.Ser397_Arg398insLysHisThr
ENST00000379328.9:c.1195_1196insAACACACCC MANE Select ENSP00000368632.3:p.Ser398_Arg399insLysHisThr
ENST00000346208.3:c.1192_1193insAACACACCC ENSP00000341619.3:p.Ser397_Arg398insLysHisThr
ENST00000379328.7:c.1195_1196insAACACACCC ENSP00000368632.3:p.Ser398_Arg399insLysHisThr
ENST00000461472.1:n.714_715insAACACACCC
NM_001002295.1:c.1195_1196insAACACACCC NP_001002295.1:p.Ser398_Arg399insLysHisThr
NM_002051.2:c.1192_1193insAACACACCC NP_002042.1:p.Ser397_Arg398insLysHisThr
XM_005252442.2:c.1195_1196insAACACACCC XP_005252499.1:p.Ser398_Arg399insLysHisThr
XM_005252443.3:c.1195_1196insAACACACCC XP_005252500.1:p.Ser398_Arg399insLysHisThr
XM_005252443.5:c.1195_1196insAACACACCC XP_005252500.1:p.Ser398_Arg399insLysHisThr
NM_001002295.2:c.1195_1196insAACACACCC MANE Select NP_001002295.1:p.Ser398_Arg399insLysHisThr
NM_002051.3:c.1192_1193insAACACACCC NP_002042.1:p.Ser397_Arg398insLysHisThr