Canonical Allele Identifier: CA1931496214

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836155_99836157delinsACT , CM000672.2:g.99836155_99836157delinsACT	GRCh38
NC_000010.10:g.101595912_101595914delinsACT , CM000672.1:g.101595912_101595914delinsACT	GRCh37
NC_000010.9:g.101585902_101585904delinsACT	NCBI36
NG_011798.1:g.58450_58452delinsACT
NG_011798.2:g.58558_58560delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3479_3481delinsACT MANE Select	ENSP00000497274.1:p.Tyr1160=
ENST00000370449.8:c.3479_3481delinsACT	ENSP00000359478.4:p.Tyr1160=
NM_000392.4:c.3479_3481delinsACT	NP_000383.1:p.Tyr1160=
XM_006717630.2:c.2783_2785delinsACT	XP_006717693.1:p.Tyr928=
XR_945604.1:n.3668_3670delinsACT
XR_945605.1:n.3670_3672delinsACT
NM_000392.5:c.3479_3481delinsACT MANE Select	NP_000383.2:p.Tyr1160=
XM_006717630.3:c.2783_2785delinsACT	XP_006717693.1:p.Tyr928=
XR_945604.3:n.3722_3724delinsACT
XR_945605.3:n.3722_3724delinsACT