Canonical Allele Identifier: CA1403099102

Gene: INHCAP TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133691829A= , CM000665.2:g.133691829A=	GRCh38
NC_000003.11:g.133410673A= , CM000665.1:g.133410673A=	GRCh37
NC_000003.10:g.134893363A=	NCBI36
NG_013080.2:g.34832A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460564.5:n.209+3465A= (INHCAP)
ENST00000475455.1:n.280A= (INHCAP)
ENST00000490470.5:n.209+3465A= (INHCAP)
ENST00000497521.5:n.208+3465A= (INHCAP)
XM_011513100.1:c.-1289+3465A= (TF)	XP_011511402.1:n.-1289+3465A=
NM_001354703.1:c.-940+3465A= (TF)	NP_001341632.1:n.-940+3465A=
NM_001354703.2:c.-940+3465A= (TF)	NP_001341632.2:n.-940+3465A=