Canonical Allele Identifier: CA1931496015

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836071_99836076delinsTCTTTA , CM000672.2:g.99836071_99836076delinsTCTTTA	GRCh38
NC_000010.10:g.101595828_101595833delinsTCTTTA , CM000672.1:g.101595828_101595833delinsTCTTTA	GRCh37
NC_000010.9:g.101585818_101585823delinsTCTTTA	NCBI36
NG_011798.1:g.58366_58371delinsTCTTTA
NG_011798.2:g.58474_58479delinsTCTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-20_3415-15delinsTCTTTA MANE Select	ENSP00000497274.1:n.3415-20_3415-15delinsTCTTTA
ENST00000370449.8:c.3415-20_3415-15delinsTCTTTA	ENSP00000359478.4:n.3415-20_3415-15delinsTCTTTA
NM_000392.4:c.3415-20_3415-15delinsTCTTTA	NP_000383.1:n.3415-20_3415-15delinsTCTTTA
XM_006717630.2:c.2719-20_2719-15delinsTCTTTA	XP_006717693.1:n.2719-20_2719-15delinsTCTTTA
XR_945604.1:n.3604-20_3604-15delinsTCTTTA
XR_945605.1:n.3606-20_3606-15delinsTCTTTA
NM_000392.5:c.3415-20_3415-15delinsTCTTTA MANE Select	NP_000383.2:n.3415-20_3415-15delinsTCTTTA
XM_006717630.3:c.2719-20_2719-15delinsTCTTTA	XP_006717693.1:n.2719-20_2719-15delinsTCTTTA
XR_945604.3:n.3658-20_3658-15delinsTCTTTA
XR_945605.3:n.3658-20_3658-15delinsTCTTTA