Canonical Allele Identifier: CA668851197

Gene: GATA3

Linked Data

• dbSNP Id: rs1255888653
• gnomAD v4: 10-8055905-G-GC
• MyVariant Identifiers: chr10:g.8097868_8097869insC (hg19) ; chr10:g.8055905_8055906insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8055908dup , CM000672.2:g.8055908dup	GRCh38
NC_000010.10:g.8097871dup , CM000672.1:g.8097871dup	GRCh37
NC_000010.9:g.8137877dup	NCBI36
NG_015859.1:g.6205dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.241+12dup	ENSP00000341619.3:n.241+12dup
ENST00000379328.9:c.241+12dup MANE Select	ENSP00000368632.3:n.241+12dup
ENST00000481743.2:c.241+12dup	ENSP00000493486.1:n.241+12dup
ENST00000346208.3:c.241+12dup	ENSP00000341619.3:n.241+12dup
ENST00000379328.7:c.241+12dup	ENSP00000368632.3:n.241+12dup
NM_001002295.1:c.241+12dup	NP_001002295.1:n.241+12dup
NM_002051.2:c.241+12dup	NP_002042.1:n.241+12dup
XM_005252442.2:c.241+12dup	XP_005252499.1:n.241+12dup
XM_005252443.3:c.241+12dup	XP_005252500.1:n.241+12dup
XM_005252443.5:c.241+12dup	XP_005252500.1:n.241+12dup
XR_001747358.1:n.617+860dup
NM_001002295.2:c.241+12dup MANE Select	NP_001002295.1:n.241+12dup
NM_002051.3:c.241+12dup	NP_002042.1:n.241+12dup