Canonical Allele Identifier: CA1931489268

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830419_99830421delinsAAC , CM000672.2:g.99830419_99830421delinsAAC	GRCh38
NC_000010.10:g.101590176_101590178delinsAAC , CM000672.1:g.101590176_101590178delinsAAC	GRCh37
NC_000010.9:g.101580166_101580168delinsAAC	NCBI36
NG_011798.1:g.52714_52716delinsAAC
NG_011798.2:g.52822_52824delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2733_2735delinsAAC MANE Select	ENSP00000497274.1:p.Arg911=
ENST00000370449.8:c.2733_2735delinsAAC	ENSP00000359478.4:p.Arg911=
NM_000392.4:c.2733_2735delinsAAC	NP_000383.1:p.Arg911=
XM_006717630.2:c.2037_2039delinsAAC	XP_006717693.1:p.Arg679=
XM_011539291.1:c.2733_2735delinsAAC	XP_011537593.1:p.Arg911=
XR_945604.1:n.2922_2924delinsAAC
XR_945605.1:n.2924_2926delinsAAC
NM_000392.5:c.2733_2735delinsAAC MANE Select	NP_000383.2:p.Arg911=
XM_006717630.3:c.2037_2039delinsAAC	XP_006717693.1:p.Arg679=
XM_011539291.3:c.2733_2735delinsAAC	XP_011537593.1:p.Arg911=
XR_945604.3:n.2976_2978delinsAAC
XR_945605.3:n.2976_2978delinsAAC