Canonical Allele Identifier: CA1403130734
Gene: TF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133775441C= , CM000665.2:g.133775441C= GRCh38
NC_000003.11:g.133494285C= , CM000665.1:g.133494285C= GRCh37
NC_000003.10:g.134976975C= NCBI36
NG_013080.1:g.34309C=
NG_013080.2:g.118444C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000402696.9:c.1696C= MANE Select ENSP00000385834.3:p.Pro566=
ENST00000402696.7:c.1696C= ENSP00000385834.3:p.Pro566=
ENST00000461695.1:c.427C=
ENST00000467842.1:n.2690C=
NM_001063.3:c.1696C= NP_001054.1:p.Pro566=
XM_011513100.1:c.1696C= XP_011511402.1:p.Pro566=
NM_001354703.1:c.1564C= NP_001341632.1:p.Pro522=
NM_001354704.1:c.1315C= NP_001341633.1:p.Pro439=
NM_001063.4:c.1696C= MANE Select NP_001054.2:p.Pro566=
NM_001354703.2:c.1564C= NP_001341632.2:p.Pro522=
NM_001354704.2:c.1315C= NP_001341633.2:p.Pro439=