Canonical Allele Identifier: CA591844072

Gene: GATA3

Linked Data

• dbSNP Id: rs1328252680
• gnomAD v2: 10-8115666-AGT-A
• gnomAD v3: 10-8073703-AGT-A
• gnomAD v4: 10-8073703-AGT-A
• MyVariant Identifiers: chr10:g.8115667_8115668del (hg19) ; chr10:g.8073704_8073705del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8073704_8073705del , CM000672.2:g.8073704_8073705del	GRCh38
NC_000010.10:g.8115667_8115668del , CM000672.1:g.8115667_8115668del	GRCh37
NC_000010.9:g.8155673_8155674del	NCBI36
NG_015859.1:g.24001_24002del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.1048-35_1048-34del	ENSP00000341619.3:n.1048-35_1048-34del
ENST00000379328.9:c.1051-35_1051-34del MANE Select	ENSP00000368632.3:n.1051-35_1051-34del
ENST00000346208.3:c.1048-35_1048-34del	ENSP00000341619.3:n.1048-35_1048-34del
ENST00000379328.7:c.1051-35_1051-34del	ENSP00000368632.3:n.1051-35_1051-34del
ENST00000461472.1:n.570-35_570-34del
NM_001002295.1:c.1051-35_1051-34del	NP_001002295.1:n.1051-35_1051-34del
NM_002051.2:c.1048-35_1048-34del	NP_002042.1:n.1048-35_1048-34del
XM_005252442.2:c.1051-35_1051-34del	XP_005252499.1:n.1051-35_1051-34del
XM_005252443.3:c.1051-35_1051-34del	XP_005252500.1:n.1051-35_1051-34del
XM_005252443.5:c.1051-35_1051-34del	XP_005252500.1:n.1051-35_1051-34del
NM_001002295.2:c.1051-35_1051-34del MANE Select	NP_001002295.1:n.1051-35_1051-34del
NM_002051.3:c.1048-35_1048-34del	NP_002042.1:n.1048-35_1048-34del