Canonical Allele Identifier: CA1931489621

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830604_99830605delinsCT , CM000672.2:g.99830604_99830605delinsCT	GRCh38
NC_000010.10:g.101590361_101590362delinsCT , CM000672.1:g.101590361_101590362delinsCT	GRCh37
NC_000010.9:g.101580351_101580352delinsCT	NCBI36
NG_011798.1:g.52899_52900delinsCT
NG_011798.2:g.53007_53008delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2748-112_2748-111delinsCT MANE Select	ENSP00000497274.1:n.2748-112_2748-111delinsCT
ENST00000370449.8:c.2748-112_2748-111delinsCT	ENSP00000359478.4:n.2748-112_2748-111delinsCT
NM_000392.4:c.2748-112_2748-111delinsCT	NP_000383.1:n.2748-112_2748-111delinsCT
XM_006717630.2:c.2052-112_2052-111delinsCT	XP_006717693.1:n.2052-112_2052-111delinsCT
XM_011539291.1:c.2747+171_2747+172delinsCT	XP_011537593.1:n.2747+171_2747+172delinsCT
XR_945604.1:n.2937-112_2937-111delinsCT
XR_945605.1:n.2939-112_2939-111delinsCT
NM_000392.5:c.2748-112_2748-111delinsCT MANE Select	NP_000383.2:n.2748-112_2748-111delinsCT
XM_006717630.3:c.2052-112_2052-111delinsCT	XP_006717693.1:n.2052-112_2052-111delinsCT
XM_011539291.3:c.2747+171_2747+172delinsCT	XP_011537593.1:n.2747+171_2747+172delinsCT
XR_945604.3:n.2991-112_2991-111delinsCT
XR_945605.3:n.2991-112_2991-111delinsCT