Canonical Allele Identifier: CA468200853

Gene: GATA3

Linked Data

• MyVariant Identifiers: chr10:g.8115986_8115987insC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8074023_8074024insC , CM000672.2:g.8074023_8074024insC	GRCh38
NC_000010.10:g.8115986_8115987insC , CM000672.1:g.8115986_8115987insC	GRCh37
NC_000010.9:g.8155992_8155993insC	NCBI36
NG_015859.1:g.24320_24321insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.1332_*1insC	ENSP00000341619.3:n.1332_*1insC
ENST00000379328.9:c.1335_*1insC MANE Select	ENSP00000368632.3:n.1335_*1insC
ENST00000346208.3:c.1332_*1insC	ENSP00000341619.3:n.1332_*1insC
ENST00000379328.7:c.1335_*1insC	ENSP00000368632.3:n.1335_*1insC
ENST00000461472.1:n.854_855insC
NM_001002295.1:c.1335_*1insC	NP_001002295.1:n.1335_*1insC
NM_002051.2:c.1332_*1insC	NP_002042.1:n.1332_*1insC
XM_005252442.2:c.1335_*1insC	XP_005252499.1:n.1335_*1insC
XM_005252443.3:c.1335_*1insC	XP_005252500.1:n.1335_*1insC
XM_005252443.5:c.1335_*1insC	XP_005252500.1:n.1335_*1insC
NM_001002295.2:c.1335_*1insC MANE Select	NP_001002295.1:n.1335_*1insC
NM_002051.3:c.1332_*1insC	NP_002042.1:n.1332_*1insC