Canonical Allele Identifier: CA1403099086

Gene: INHCAP TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133691790G= , CM000665.2:g.133691790G=	GRCh38
NC_000003.11:g.133410634G= , CM000665.1:g.133410634G=	GRCh37
NC_000003.10:g.134893324G=	NCBI36
NG_013080.2:g.34793G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460564.5:n.209+3426G= (INHCAP)
ENST00000475455.1:n.241G= (INHCAP)
ENST00000490470.5:n.209+3426G= (INHCAP)
ENST00000497521.5:n.208+3426G= (INHCAP)
XM_011513100.1:c.-1289+3426G= (TF)	XP_011511402.1:n.-1289+3426G=
NM_001354703.1:c.-940+3426G= (TF)	NP_001341632.1:n.-940+3426G=
NM_001354703.2:c.-940+3426G= (TF)	NP_001341632.2:n.-940+3426G=