Canonical Allele Identifier: CA1931495865
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99835896_99835898delinsCCA , CM000672.2:g.99835896_99835898delinsCCA GRCh38
NC_000010.10:g.101595653_101595655delinsCCA , CM000672.1:g.101595653_101595655delinsCCA GRCh37
NC_000010.9:g.101585643_101585645delinsCCA NCBI36
NG_011798.1:g.58191_58193delinsCCA
NG_011798.2:g.58299_58301delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3415-195_3415-193delinsCCA MANE Select ENSP00000497274.1:n.3415-195_3415-193delinsCCA
ENST00000370449.8:c.3415-195_3415-193delinsCCA ENSP00000359478.4:n.3415-195_3415-193delinsCCA
NM_000392.4:c.3415-195_3415-193delinsCCA NP_000383.1:n.3415-195_3415-193delinsCCA
XM_006717630.2:c.2719-195_2719-193delinsCCA XP_006717693.1:n.2719-195_2719-193delinsCCA
XR_945604.1:n.3604-195_3604-193delinsCCA
XR_945605.1:n.3606-195_3606-193delinsCCA
NM_000392.5:c.3415-195_3415-193delinsCCA MANE Select NP_000383.2:n.3415-195_3415-193delinsCCA
XM_006717630.3:c.2719-195_2719-193delinsCCA XP_006717693.1:n.2719-195_2719-193delinsCCA
XR_945604.3:n.3658-195_3658-193delinsCCA
XR_945605.3:n.3658-195_3658-193delinsCCA