Canonical Allele Identifier: CA2260418235
Community Standard Title: NM_001288718.2(STAT5A):c.376-1215C=
Gene: STAT5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42294404C= , CM000679.2:g.42294404C= GRCh38
NC_000017.10:g.40446422C= , CM000679.1:g.40446422C= GRCh37
NC_000017.9:g.37699948C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001288718.2:c.376-1215C= MANE Select NP_001275647.1:n.376-1215C=
ENST00000590949.6:c.376-1215C= MANE Select ENSP00000468749.1:n.376-1215C=
NM_001288718.1:c.376-1215C= NP_001275647.1:n.376-1215C=
NM_001288719.1:c.286-1215C= NP_001275648.1:n.286-1215C=
NM_001288719.2:c.286-1215C= NP_001275648.1:n.286-1215C=
NM_001288720.1:c.376-1215C= NP_001275649.1:n.376-1215C=
NM_001288720.2:c.376-1215C= NP_001275649.1:n.376-1215C=
NM_003152.3:c.376-1215C= NP_003143.2:n.376-1215C=
NM_003152.4:c.376-1215C= NP_003143.2:n.376-1215C=
ENST00000345506.8:c.376-1215C= ENSP00000341208.4:n.376-1215C=
ENST00000546010.6:c.286-1215C= ENSP00000443107.1:n.286-1215C=
ENST00000588868.5:c.376-1215C= ENSP00000465437.1:n.376-1215C=
ENST00000590726.6:c.-33-1215C= ENSP00000464730.2:n.-33-1215C=
ENST00000590726.7:c.-33-1215C= ENSP00000464730.3:n.-33-1215C=
ENST00000590949.5:c.376-1215C= ENSP00000468749.1:n.376-1215C=
ENST00000676585.1:c.376-1215C= ENSP00000504449.1:n.376-1215C=
ENST00000676631.1:c.376-1215C= ENSP00000503484.1:n.376-1215C=
ENST00000677301.1:c.376-1215C= ENSP00000503262.1:n.376-1215C=
ENST00000677893.1:c.376-1215C= ENSP00000504833.1:n.376-1215C=
ENST00000678903.1:c.325-1215C= ENSP00000503304.1:n.325-1215C=
XM_005257624.2:c.376-1215C= XP_005257681.1:n.376-1215C=
XM_005257624.3:c.376-1215C= XP_005257681.1:n.376-1215C=