Canonical Allele Identifier: CA1931489549

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830550_99830554delinsCCTTT , CM000672.2:g.99830550_99830554delinsCCTTT	GRCh38
NC_000010.10:g.101590307_101590311delinsCCTTT , CM000672.1:g.101590307_101590311delinsCCTTT	GRCh37
NC_000010.9:g.101580297_101580301delinsCCTTT	NCBI36
NG_011798.1:g.52845_52849delinsCCTTT
NG_011798.2:g.52953_52957delinsCCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2747+117_2747+121delinsCCTTT MANE Select	ENSP00000497274.1:n.2747+117_2747+121delinsCCTTT
ENST00000370449.8:c.2747+117_2747+121delinsCCTTT	ENSP00000359478.4:n.2747+117_2747+121delinsCCTTT
NM_000392.4:c.2747+117_2747+121delinsCCTTT	NP_000383.1:n.2747+117_2747+121delinsCCTTT
XM_006717630.2:c.2051+117_2051+121delinsCCTTT	XP_006717693.1:n.2051+117_2051+121delinsCCTTT
XM_011539291.1:c.2747+117_2747+121delinsCCTTT	XP_011537593.1:n.2747+117_2747+121delinsCCTTT
XR_945604.1:n.2936+117_2936+121delinsCCTTT
XR_945605.1:n.2938+117_2938+121delinsCCTTT
NM_000392.5:c.2747+117_2747+121delinsCCTTT MANE Select	NP_000383.2:n.2747+117_2747+121delinsCCTTT
XM_006717630.3:c.2051+117_2051+121delinsCCTTT	XP_006717693.1:n.2051+117_2051+121delinsCCTTT
XM_011539291.3:c.2747+117_2747+121delinsCCTTT	XP_011537593.1:n.2747+117_2747+121delinsCCTTT
XR_945604.3:n.2990+117_2990+121delinsCCTTT
XR_945605.3:n.2990+117_2990+121delinsCCTTT