Canonical Allele Identifier: CA1403099078

Gene: INHCAP TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133691772C= , CM000665.2:g.133691772C=	GRCh38
NC_000003.11:g.133410616C= , CM000665.1:g.133410616C=	GRCh37
NC_000003.10:g.134893306C=	NCBI36
NG_013080.2:g.34775C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460564.5:n.209+3408C= (INHCAP)
ENST00000475455.1:n.223C= (INHCAP)
ENST00000490470.5:n.209+3408C= (INHCAP)
ENST00000497521.5:n.208+3408C= (INHCAP)
XM_011513100.1:c.-1289+3408C= (TF)	XP_011511402.1:n.-1289+3408C=
NM_001354703.1:c.-940+3408C= (TF)	NP_001341632.1:n.-940+3408C=
NM_001354703.2:c.-940+3408C= (TF)	NP_001341632.2:n.-940+3408C=