Canonical Allele Identifier: CA5404359

Gene: GATA3

Linked Data

• dbSNP Id: rs773322691
• ExAC: 10:8100434 CTCG / C
• gnomAD v2: 10-8100434-CTCG-C
• gnomAD v4: 10-8058471-CTCG-C
• MyVariant Identifiers: chr10:g.8100435_8100437del (hg19) ; chr10:g.8058472_8058474del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8058474_8058476del , CM000672.2:g.8058474_8058476del	GRCh38
NC_000010.10:g.8100437_8100439del , CM000672.1:g.8100437_8100439del	GRCh37
NC_000010.9:g.8140443_8140445del	NCBI36
NG_015859.1:g.8771_8773del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.411_413del	ENSP00000341619.3:p.Ser138del
ENST00000379328.9:c.411_413del MANE Select	ENSP00000368632.3:p.Ser138del
ENST00000481743.2:c.411_413del	ENSP00000493486.1:p.Ser138del
ENST00000346208.3:c.411_413del	ENSP00000341619.3:p.Ser138del
ENST00000379328.7:c.411_413del	ENSP00000368632.3:p.Ser138del
ENST00000461472.1:n.76_78del
NM_001002295.1:c.411_413del	NP_001002295.1:p.Ser138del
NM_002051.2:c.411_413del	NP_002042.1:p.Ser138del
XM_005252442.2:c.411_413del	XP_005252499.1:p.Ser138del
XM_005252443.3:c.411_413del	XP_005252500.1:p.Ser138del
XM_005252443.5:c.411_413del	XP_005252500.1:p.Ser138del
NM_001002295.2:c.411_413del MANE Select	NP_001002295.1:p.Ser138del
NM_002051.3:c.411_413del	NP_002042.1:p.Ser138del