Canonical Allele Identifier: CA202455312

Gene: GATA3

Linked Data

• dbSNP Id: rs145573634
• MyVariant Identifiers: chr10:g.8100337_8100338insC (hg19) ; chr10:g.8058374_8058375insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8058375dup , CM000672.2:g.8058375dup	GRCh38
NC_000010.10:g.8100338dup , CM000672.1:g.8100338dup	GRCh37
NC_000010.9:g.8140344dup	NCBI36
NG_015859.1:g.8672dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.312dup	ENSP00000341619.3:p.Ser105GlnfsTer?
ENST00000379328.9:c.312dup MANE Select	ENSP00000368632.3:p.Ser105GlnfsTer?
ENST00000481743.2:c.312dup	ENSP00000493486.1:p.Ser105GlnfsTer?
ENST00000346208.3:c.312dup	ENSP00000341619.3:p.Ser105GlnfsTer?
ENST00000379328.7:c.312dup	ENSP00000368632.3:p.Ser105GlnfsTer?
NM_001002295.1:c.312dup	NP_001002295.1:p.Ser105GlnfsTer?
NM_002051.2:c.312dup	NP_002042.1:p.Ser105GlnfsTer?
XM_005252442.2:c.312dup	XP_005252499.1:p.Ser105GlnfsTer?
XM_005252443.3:c.312dup	XP_005252500.1:p.Ser105GlnfsTer?
XM_005252443.5:c.312dup	XP_005252500.1:p.Ser105GlnfsTer?
NM_001002295.2:c.312dup MANE Select	NP_001002295.1:p.Ser105GlnfsTer?
NM_002051.3:c.312dup	NP_002042.1:p.Ser105GlnfsTer?