Canonical Allele Identifier: CA1931495725

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99835759_99835761delinsCTG , CM000672.2:g.99835759_99835761delinsCTG	GRCh38
NC_000010.10:g.101595516_101595518delinsCTG , CM000672.1:g.101595516_101595518delinsCTG	GRCh37
NC_000010.9:g.101585506_101585508delinsCTG	NCBI36
NG_011798.1:g.58054_58056delinsCTG
NG_011798.2:g.58162_58164delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-332_3415-330delinsCTG MANE Select	ENSP00000497274.1:n.3415-332_3415-330delinsCTG
ENST00000370449.8:c.3415-332_3415-330delinsCTG	ENSP00000359478.4:n.3415-332_3415-330delinsCTG
NM_000392.4:c.3415-332_3415-330delinsCTG	NP_000383.1:n.3415-332_3415-330delinsCTG
XM_006717630.2:c.2719-332_2719-330delinsCTG	XP_006717693.1:n.2719-332_2719-330delinsCTG
XR_945604.1:n.3604-332_3604-330delinsCTG
XR_945605.1:n.3606-332_3606-330delinsCTG
NM_000392.5:c.3415-332_3415-330delinsCTG MANE Select	NP_000383.2:n.3415-332_3415-330delinsCTG
XM_006717630.3:c.2719-332_2719-330delinsCTG	XP_006717693.1:n.2719-332_2719-330delinsCTG
XR_945604.3:n.3658-332_3658-330delinsCTG
XR_945605.3:n.3658-332_3658-330delinsCTG