Canonical Allele Identifier: CA7052682

Gene: ING1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110715817G>A , CM000675.2:g.110715817G>A	GRCh38
NG_042045.2:g.2785C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375775.4:c.-72+2231G>A	ENSP00000364930.3:n.-72+2231G>A
ENST00000333219.9:c.136+1532G>A MANE Select	ENSP00000328436.8:n.136+1532G>A
ENST00000333219.8:c.136+1532G>A	ENSP00000328436.7:n.136+1532G>A
ENST00000338450.7:c.4+2840G>A	ENSP00000345202.7:n.4+2840G>A
ENST00000375774.3:c.374G>A	ENSP00000364929.3:p.Arg125Gln
ENST00000375775.3:c.-72+2231G>A	ENSP00000364930.3:n.-72+2231G>A
ENST00000464141.1:c.85+289G>A	ENSP00000480985.1:n.85+289G>A
NM_001267728.1:c.85+289G>A	NP_001254657.1:n.85+289G>A
NM_005537.5:c.374G>A	NP_005528.4:p.Arg125Gln
NM_198217.2:c.4+2840G>A	NP_937860.1:n.4+2840G>A
NM_198218.2:c.-72+2231G>A	NP_937861.1:n.-72+2231G>A
NM_198219.2:c.136+1532G>A	NP_937862.1:n.136+1532G>A
NM_198219.3:c.136+1532G>A MANE Select	NP_937862.1:n.136+1532G>A
NM_198217.3:c.4+2840G>A	NP_937860.1:n.4+2840G>A
NM_198218.3:c.-72+2231G>A	NP_937861.1:n.-72+2231G>A