Canonical Allele Identifier: CA388749679

Gene: ING1

Linked Data

• MyVariant Identifiers: chr13:g.111372082T>A (hg19) ; chr13:g.110719735T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110719735T>A , CM000675.2:g.110719735T>A	GRCh38
NC_000013.10:g.111372082T>A , CM000675.1:g.111372082T>A	GRCh37
NC_000013.9:g.110170083T>A	NCBI36
NG_012197.1:g.12000T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375775.4:c.436T>A	ENSP00000364930.3:p.Cys146Ser
ENST00000333219.9:c.643T>A MANE Select	ENSP00000328436.8:p.Cys215Ser
ENST00000333219.8:c.643T>A	ENSP00000328436.7:p.Cys215Ser
ENST00000338450.7:c.511T>A	ENSP00000345202.7:p.Cys171Ser
ENST00000375774.3:c.1072T>A	ENSP00000364929.3:p.Cys358Ser
ENST00000375775.3:c.436T>A	ENSP00000364930.3:p.Cys146Ser
NM_001267728.1:c.592T>A	NP_001254657.1:p.Cys198Ser
NM_005537.5:c.1072T>A	NP_005528.4:p.Cys358Ser
NM_198217.2:c.511T>A	NP_937860.1:p.Cys171Ser
NM_198218.2:c.436T>A	NP_937861.1:p.Cys146Ser
NM_198219.2:c.643T>A	NP_937862.1:p.Cys215Ser
NM_198219.3:c.643T>A MANE Select	NP_937862.1:p.Cys215Ser
NM_198217.3:c.511T>A	NP_937860.1:p.Cys171Ser
NM_198218.3:c.436T>A	NP_937861.1:p.Cys146Ser