Canonical Allele Identifier: CA11558137

Gene: INHCAP TF

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133744613G>A , CM000665.2:g.133744613G>A	GRCh38
NC_000003.11:g.133463457G>A , CM000665.1:g.133463457G>A	GRCh37
NC_000003.10:g.134946147G>A	NCBI36
NG_013080.1:g.3481G>A
NG_013080.2:g.87616G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460564.5:n.382-8982G>A (INHCAP)
XM_011513100.1:c.-438-1390G>A (TF)	XP_011511402.1:n.-438-1390G>A
NM_001354703.1:c.-89-3799G>A (TF)	NP_001341632.1:n.-89-3799G>A
NM_001354703.2:c.-89-3799G>A (TF)	NP_001341632.2:n.-89-3799G>A