Canonical Allele Identifier: CA1889012645

Gene: GATA3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8058471_8058474delinsCTCG , CM000672.2:g.8058471_8058474delinsCTCG	GRCh38
NC_000010.10:g.8100434_8100437delinsCTCG , CM000672.1:g.8100434_8100437delinsCTCG	GRCh37
NC_000010.9:g.8140440_8140443delinsCTCG	NCBI36
NG_015859.1:g.8768_8771delinsCTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.408_411delinsCTCG	ENSP00000341619.3:p.Ala136=
ENST00000379328.9:c.408_411delinsCTCG MANE Select	ENSP00000368632.3:p.Ala136=
ENST00000481743.2:c.408_411delinsCTCG	ENSP00000493486.1:p.Ala136=
ENST00000346208.3:c.408_411delinsCTCG	ENSP00000341619.3:p.Ala136=
ENST00000379328.7:c.408_411delinsCTCG	ENSP00000368632.3:p.Ala136=
ENST00000461472.1:n.73_76delinsCTCG
NM_001002295.1:c.408_411delinsCTCG	NP_001002295.1:p.Ala136=
NM_002051.2:c.408_411delinsCTCG	NP_002042.1:p.Ala136=
XM_005252442.2:c.408_411delinsCTCG	XP_005252499.1:p.Ala136=
XM_005252443.3:c.408_411delinsCTCG	XP_005252500.1:p.Ala136=
XM_005252443.5:c.408_411delinsCTCG	XP_005252500.1:p.Ala136=
NM_001002295.2:c.408_411delinsCTCG MANE Select	NP_001002295.1:p.Ala136=
NM_002051.3:c.408_411delinsCTCG	NP_002042.1:p.Ala136=