Canonical Allele Identifier: CA2210069800

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16034940_16034952delinsTGTTTGTGTGTGC , CM000678.2:g.16034940_16034952delinsTGTTTGTGTGTGC	GRCh38
NC_000016.9:g.16128797_16128809delinsTGTTTGTGTGTGC , CM000678.1:g.16128797_16128809delinsTGTTTGTGTGTGC	GRCh37
NC_000016.8:g.16036298_16036310delinsTGTTTGTGTGTGC	NCBI36
NG_028268.1:g.90364_90376delinsTGTTTGTGTGTGC
NG_028268.2:g.90364_90376delinsTGTTTGTGTGTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.678-1532_678-1520delinsTGTTTGTGTGTGC	ENSP00000382340.4:n.678-1532_678-1520delinsTGTTTGTGTGTGC
ENST00000399410.8:c.678-1532_678-1520delinsTGTTTGTGTGTGC MANE Select	ENSP00000382342.3:n.678-1532_678-1520delinsTGTTTGTGTGTGC
ENST00000572882.3:c.678-1532_678-1520delinsTGTTTGTGTGTGC	ENSP00000461615.2:n.678-1532_678-1520delinsTGTTTGTGTGTGC
ENST00000574224.2:n.753-1532_753-1520delinsTGTTTGTGTGTGC
ENST00000677164.1:c.552-1532_552-1520delinsTGTTTGTGTGTGC	ENSP00000502873.1:n.552-1532_552-1520delinsTGTTTGTGTGTGC
ENST00000678422.1:c.678-1532_678-1520delinsTGTTTGTGTGTGC	ENSP00000503954.1:n.678-1532_678-1520delinsTGTTTGTGTGTGC
ENST00000679043.1:n.630-1532_630-1520delinsTGTTTGTGTGTGC
ENST00000399408.6:c.-301-1532_-301-1520delinsTGTTTGTGTGTGC	ENSP00000382340.3:n.-301-1532_-301-1520delinsTGTTTGTGTGTGC
ENST00000399410.7:c.678-1532_678-1520delinsTGTTTGTGTGTGC	ENSP00000382342.3:n.678-1532_678-1520delinsTGTTTGTGTGTGC
ENST00000572882.2:c.373-1532_373-1520delinsTGTTTGTGTGTGC
ENST00000574224.1:n.278-1532_278-1520delinsTGTTTGTGTGTGC
NM_004996.3:c.678-1532_678-1520delinsTGTTTGTGTGTGC	NP_004987.2:n.678-1532_678-1520delinsTGTTTGTGTGTGC
XM_011522497.1:c.654-1532_654-1520delinsTGTTTGTGTGTGC	XP_011520799.1:n.654-1532_654-1520delinsTGTTTGTGTGTGC
XM_011522498.1:c.732-1532_732-1520delinsTGTTTGTGTGTGC	XP_011520800.1:n.732-1532_732-1520delinsTGTTTGTGTGTGC
XM_011522498.2:c.732-1532_732-1520delinsTGTTTGTGTGTGC	XP_011520800.1:n.732-1532_732-1520delinsTGTTTGTGTGTGC
XM_017023237.1:c.732-1532_732-1520delinsTGTTTGTGTGTGC	XP_016878726.1:n.732-1532_732-1520delinsTGTTTGTGTGTGC
XM_017023238.1:c.606-1532_606-1520delinsTGTTTGTGTGTGC	XP_016878727.1:n.606-1532_606-1520delinsTGTTTGTGTGTGC
XM_017023239.1:c.594-1532_594-1520delinsTGTTTGTGTGTGC	XP_016878728.1:n.594-1532_594-1520delinsTGTTTGTGTGTGC
XM_017023240.1:c.732-1532_732-1520delinsTGTTTGTGTGTGC	XP_016878729.1:n.732-1532_732-1520delinsTGTTTGTGTGTGC
XM_017023241.1:c.468-1532_468-1520delinsTGTTTGTGTGTGC	XP_016878730.1:n.468-1532_468-1520delinsTGTTTGTGTGTGC
XM_017023242.1:c.732-1532_732-1520delinsTGTTTGTGTGTGC	XP_016878731.1:n.732-1532_732-1520delinsTGTTTGTGTGTGC
XM_017023243.2:c.732-1532_732-1520delinsTGTTTGTGTGTGC	XP_016878732.1:n.732-1532_732-1520delinsTGTTTGTGTGTGC
NM_004996.4:c.678-1532_678-1520delinsTGTTTGTGTGTGC MANE Select	NP_004987.2:n.678-1532_678-1520delinsTGTTTGTGTGTGC