Canonical Allele Identifier: CA468401144

Gene: GATA3

Linked Data

• MyVariant Identifiers: chr10:g.8115947_8115948insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8073984_8073985insG , CM000672.2:g.8073984_8073985insG	GRCh38
NC_000010.10:g.8115947_8115948insG , CM000672.1:g.8115947_8115948insG	GRCh37
NC_000010.9:g.8155953_8155954insG	NCBI36
NG_015859.1:g.24281_24282insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.1293_1294insG	ENSP00000341619.3:p.Pro432AlafsTer?
ENST00000379328.9:c.1296_1297insG MANE Select	ENSP00000368632.3:p.Pro433AlafsTer?
ENST00000346208.3:c.1293_1294insG	ENSP00000341619.3:p.Pro432AlafsTer?
ENST00000379328.7:c.1296_1297insG	ENSP00000368632.3:p.Pro433AlafsTer?
ENST00000461472.1:n.815_816insG
NM_001002295.1:c.1296_1297insG	NP_001002295.1:p.Pro433AlafsTer?
NM_002051.2:c.1293_1294insG	NP_002042.1:p.Pro432AlafsTer?
XM_005252442.2:c.1296_1297insG	XP_005252499.1:p.Pro433AlafsTer?
XM_005252443.3:c.1296_1297insG	XP_005252500.1:p.Pro433AlafsTer?
XM_005252443.5:c.1296_1297insG	XP_005252500.1:p.Pro433AlafsTer?
NM_001002295.2:c.1296_1297insG MANE Select	NP_001002295.1:p.Pro433AlafsTer?
NM_002051.3:c.1293_1294insG	NP_002042.1:p.Pro432AlafsTer?