Canonical Allele Identifier: CA2574661871

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845533_99845534del , CM000672.2:g.99845533_99845534del	GRCh38
NC_000010.10:g.101605290_101605291del , CM000672.1:g.101605290_101605291del	GRCh37
NC_000010.9:g.101595280_101595281del	NCBI36
NG_011798.1:g.67828_67829del
NG_011798.2:g.67936_67937del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3988-91_3988-90del MANE Select	ENSP00000497274.1:n.3988-91_3988-90del
ENST00000649459.1:n.336-91_336-90del
ENST00000370449.8:c.3988-91_3988-90del	ENSP00000359478.4:n.3988-91_3988-90del
NM_000392.4:c.3988-91_3988-90del	NP_000383.1:n.3988-91_3988-90del
XM_006717630.2:c.3292-91_3292-90del	XP_006717693.1:n.3292-91_3292-90del
XR_945604.1:n.4177-150_4177-149del
XR_945605.1:n.4052-91_4052-90del
NM_000392.5:c.3988-91_3988-90del MANE Select	NP_000383.2:n.3988-91_3988-90del
XM_006717630.3:c.3292-91_3292-90del	XP_006717693.1:n.3292-91_3292-90del
XR_945604.3:n.4231-150_4231-149del
XR_945605.3:n.4104-91_4104-90del