Canonical Allele Identifier: CA1882578611

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255392_133255396delinsCTGTG , CM000671.2:g.133255392_133255396delinsCTGTG	GRCh38
NC_000009.11:g.136130779_136130783delinsCTGTG , CM000671.1:g.136130779_136130783delinsCTGTG	GRCh37
NC_000009.10:g.135120600_135120604delinsCTGTG	NCBI36
NG_006669.1:g.22272_22276delinsCACAG
NG_006669.2:g.24820_24824delinsCACAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1364_1368delinsCACAG
ENST00000647353.1:n.54-4244_54-4240delinsCACAG
ENST00000679909.1:c.28+19766_28+19770delinsCACAG	ENSP00000506089.1:n.28+19766_28+19770delinsCACAG
ENST00000453660.3:n.1346_1350delinsCACAG
ENST00000611156.4:c.*270_*274delinsCACAG	ENSP00000483265.1:n.*270_*274delinsCACAG
NM_020469.2:c.*270_*274delinsCACAG	NP_065202.2:n.*270_*274delinsCACAG
NM_020469.3:c.*270_*274delinsCACAG	NP_065202.2:n.*270_*274delinsCACAG