Canonical Allele Identifier: CA1931514080

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845744_99845745delinsCT , CM000672.2:g.99845744_99845745delinsCT	GRCh38
NC_000010.10:g.101605501_101605502delinsCT , CM000672.1:g.101605501_101605502delinsCT	GRCh37
NC_000010.9:g.101595491_101595492delinsCT	NCBI36
NG_011798.1:g.68039_68040delinsCT
NG_011798.2:g.68147_68148delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4108_4109delinsCT MANE Select	ENSP00000497274.1:p.Leu1370=
ENST00000649459.1:n.456_457delinsCT
ENST00000370449.8:c.4108_4109delinsCT	ENSP00000359478.4:p.Leu1370=
NM_000392.4:c.4108_4109delinsCT	NP_000383.1:p.Leu1370=
XM_006717630.2:c.3412_3413delinsCT	XP_006717693.1:p.Leu1138=
XR_945604.1:n.4238_4239delinsCT
XR_945605.1:n.4172_4173delinsCT
NM_000392.5:c.4108_4109delinsCT MANE Select	NP_000383.2:p.Leu1370=
XM_006717630.3:c.3412_3413delinsCT	XP_006717693.1:p.Leu1138=
XR_945604.3:n.4292_4293delinsCT
XR_945605.3:n.4224_4225delinsCT