Canonical Allele Identifier: CA1889013067

Gene: GATA3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8058573_8058582delinsAGGCTCGGCC , CM000672.2:g.8058573_8058582delinsAGGCTCGGCC	GRCh38
NC_000010.10:g.8100536_8100545delinsAGGCTCGGCC , CM000672.1:g.8100536_8100545delinsAGGCTCGGCC	GRCh37
NC_000010.9:g.8140542_8140551delinsAGGCTCGGCC	NCBI36
NG_015859.1:g.8870_8879delinsAGGCTCGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.510_519delinsAGGCTCGGCC	ENSP00000341619.3:p.Pro170=
ENST00000379328.9:c.510_519delinsAGGCTCGGCC MANE Select	ENSP00000368632.3:p.Pro170=
ENST00000346208.3:c.510_519delinsAGGCTCGGCC	ENSP00000341619.3:p.Pro170=
ENST00000379328.7:c.510_519delinsAGGCTCGGCC	ENSP00000368632.3:p.Pro170=
ENST00000461472.1:n.175_184delinsAGGCTCGGCC
NM_001002295.1:c.510_519delinsAGGCTCGGCC	NP_001002295.1:p.Pro170=
NM_002051.2:c.510_519delinsAGGCTCGGCC	NP_002042.1:p.Pro170=
XM_005252442.2:c.510_519delinsAGGCTCGGCC	XP_005252499.1:p.Pro170=
XM_005252443.3:c.510_519delinsAGGCTCGGCC	XP_005252500.1:p.Pro170=
XM_005252443.5:c.510_519delinsAGGCTCGGCC	XP_005252500.1:p.Pro170=
NM_001002295.2:c.510_519delinsAGGCTCGGCC MANE Select	NP_001002295.1:p.Pro170=
NM_002051.3:c.510_519delinsAGGCTCGGCC	NP_002042.1:p.Pro170=