Canonical Allele Identifier: CA1403102132

Gene: TF INHCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133753607G= , CM000665.2:g.133753607G=	GRCh38
NC_000003.11:g.133472451G= , CM000665.1:g.133472451G=	GRCh37
NC_000003.10:g.134955141G=	NCBI36
NG_013080.1:g.12475G=
NG_013080.2:g.96610G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001063.4:c.229G= (TF) MANE Select	NP_001054.2:p.Asp77=
ENST00000402696.9:c.229G= (TF) MANE Select	ENSP00000385834.3:p.Asp77=
NM_001063.3:c.229G= (TF)	NP_001054.1:p.Asp77=
NM_001354703.1:c.97G= (TF)	NP_001341632.1:p.Asp33=
NM_001354703.2:c.97G= (TF)	NP_001341632.2:p.Asp33=
NM_001354704.1:c.-153G= (TF)	NP_001341633.1:n.-153G=
NM_001354704.2:c.-153G= (TF)	NP_001341633.2:n.-153G=
ENST00000402696.7:c.229G= (TF)	ENSP00000385834.3:p.Asp77=
ENST00000414694.5:c.314G= (TF)	ENSP00000401505.1:p.Gly105=
ENST00000460531.5:n.104G= (TF)
ENST00000460564.5:n.394G= (INHCAP)
ENST00000466911.5:c.97G= (TF)	ENSP00000417468.1:p.Asp33=
ENST00000474287.5:n.342G= (TF)
ENST00000475382.5:n.321G= (TF)
ENST00000482271.5:c.-153G= (TF)	ENSP00000419338.1:n.-153G=
ENST00000485977.1:c.158-3325G= (TF)	ENSP00000418716.1:n.158-3325G=
ENST00000493011.5:n.277G= (TF)
ENST00000494430.5:c.229G= (TF)	ENSP00000418396.1:p.Asp77=
ENST00000498622.1:n.458G= (TF)
XM_011513100.1:c.229G= (TF)	XP_011511402.1:p.Asp77=