Canonical Allele Identifier: CA2695211813
Gene: GATA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8058712_8058716delinsAAA , CM000672.2:g.8058712_8058716delinsAAA GRCh38
NC_000010.10:g.8100675_8100679delinsAAA , CM000672.1:g.8100675_8100679delinsAAA GRCh37
NC_000010.9:g.8140681_8140685delinsAAA NCBI36
NG_015859.1:g.9009_9013delinsAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000346208.4:c.649_653delinsAAA ENSP00000341619.3:p.His217LysfsTer?
ENST00000379328.9:c.649_653delinsAAA MANE Select ENSP00000368632.3:p.His217LysfsTer?
ENST00000346208.3:c.649_653delinsAAA ENSP00000341619.3:p.His217LysfsTer?
ENST00000379328.7:c.649_653delinsAAA ENSP00000368632.3:p.His217LysfsTer?
ENST00000461472.1:n.314_318delinsAAA
NM_001002295.1:c.649_653delinsAAA NP_001002295.1:p.His217LysfsTer?
NM_002051.2:c.649_653delinsAAA NP_002042.1:p.His217LysfsTer?
XM_005252442.2:c.649_653delinsAAA XP_005252499.1:p.His217LysfsTer?
XM_005252443.3:c.649_653delinsAAA XP_005252500.1:p.His217LysfsTer?
XM_005252443.5:c.649_653delinsAAA XP_005252500.1:p.His217LysfsTer?
NM_001002295.2:c.649_653delinsAAA MANE Select NP_001002295.1:p.His217LysfsTer?
NM_002051.3:c.649_653delinsAAA NP_002042.1:p.His217LysfsTer?