Canonical Allele Identifier: CA1931489294

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830434_99830441delinsGTTGGCTA , CM000672.2:g.99830434_99830441delinsGTTGGCTA	GRCh38
NC_000010.10:g.101590191_101590198delinsGTTGGCTA , CM000672.1:g.101590191_101590198delinsGTTGGCTA	GRCh37
NC_000010.9:g.101580181_101580188delinsGTTGGCTA	NCBI36
NG_011798.1:g.52729_52736delinsGTTGGCTA
NG_011798.2:g.52837_52844delinsGTTGGCTA

Transcript Alleles

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