Canonical Allele Identifier: CA1931496140

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836131_99836133delinsACT , CM000672.2:g.99836131_99836133delinsACT	GRCh38
NC_000010.10:g.101595888_101595890delinsACT , CM000672.1:g.101595888_101595890delinsACT	GRCh37
NC_000010.9:g.101585878_101585880delinsACT	NCBI36
NG_011798.1:g.58426_58428delinsACT
NG_011798.2:g.58534_58536delinsACT

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3455_3457delinsACT MANE Select	ENSP00000497274.1:p.Asp1152=
ENST00000370449.8:c.3455_3457delinsACT	ENSP00000359478.4:p.Asp1152=
NM_000392.4:c.3455_3457delinsACT	NP_000383.1:p.Asp1152=
XM_006717630.2:c.2759_2761delinsACT	XP_006717693.1:p.Asp920=
XR_945604.1:n.3644_3646delinsACT
XR_945605.1:n.3646_3648delinsACT
NM_000392.5:c.3455_3457delinsACT MANE Select	NP_000383.2:p.Asp1152=
XM_006717630.3:c.2759_2761delinsACT	XP_006717693.1:p.Asp920=
XR_945604.3:n.3698_3700delinsACT
XR_945605.3:n.3698_3700delinsACT