Canonical Allele Identifier: CA1931495699

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99835743_99835746delinsCTAA , CM000672.2:g.99835743_99835746delinsCTAA	GRCh38
NC_000010.10:g.101595500_101595503delinsCTAA , CM000672.1:g.101595500_101595503delinsCTAA	GRCh37
NC_000010.9:g.101585490_101585493delinsCTAA	NCBI36
NG_011798.1:g.58038_58041delinsCTAA
NG_011798.2:g.58146_58149delinsCTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-348_3415-345delinsCTAA MANE Select	ENSP00000497274.1:n.3415-348_3415-345delinsCTAA
ENST00000370449.8:c.3415-348_3415-345delinsCTAA	ENSP00000359478.4:n.3415-348_3415-345delinsCTAA
NM_000392.4:c.3415-348_3415-345delinsCTAA	NP_000383.1:n.3415-348_3415-345delinsCTAA
XM_006717630.2:c.2719-348_2719-345delinsCTAA	XP_006717693.1:n.2719-348_2719-345delinsCTAA
XR_945604.1:n.3604-348_3604-345delinsCTAA
XR_945605.1:n.3606-348_3606-345delinsCTAA
NM_000392.5:c.3415-348_3415-345delinsCTAA MANE Select	NP_000383.2:n.3415-348_3415-345delinsCTAA
XM_006717630.3:c.2719-348_2719-345delinsCTAA	XP_006717693.1:n.2719-348_2719-345delinsCTAA
XR_945604.3:n.3658-348_3658-345delinsCTAA
XR_945605.3:n.3658-348_3658-345delinsCTAA