Canonical Allele Identifier: CA1931489447

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830508_99830509delinsCT , CM000672.2:g.99830508_99830509delinsCT	GRCh38
NC_000010.10:g.101590265_101590266delinsCT , CM000672.1:g.101590265_101590266delinsCT	GRCh37
NC_000010.9:g.101580255_101580256delinsCT	NCBI36
NG_011798.1:g.52803_52804delinsCT
NG_011798.2:g.52911_52912delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2747+75_2747+76delinsCT MANE Select	ENSP00000497274.1:n.2747+75_2747+76delinsCT
ENST00000370449.8:c.2747+75_2747+76delinsCT	ENSP00000359478.4:n.2747+75_2747+76delinsCT
NM_000392.4:c.2747+75_2747+76delinsCT	NP_000383.1:n.2747+75_2747+76delinsCT
XM_006717630.2:c.2051+75_2051+76delinsCT	XP_006717693.1:n.2051+75_2051+76delinsCT
XM_011539291.1:c.2747+75_2747+76delinsCT	XP_011537593.1:n.2747+75_2747+76delinsCT
XR_945604.1:n.2936+75_2936+76delinsCT
XR_945605.1:n.2938+75_2938+76delinsCT
NM_000392.5:c.2747+75_2747+76delinsCT MANE Select	NP_000383.2:n.2747+75_2747+76delinsCT
XM_006717630.3:c.2051+75_2051+76delinsCT	XP_006717693.1:n.2051+75_2051+76delinsCT
XM_011539291.3:c.2747+75_2747+76delinsCT	XP_011537593.1:n.2747+75_2747+76delinsCT
XR_945604.3:n.2990+75_2990+76delinsCT
XR_945605.3:n.2990+75_2990+76delinsCT