Canonical Allele Identifier: CA2789199743

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844215_99844217del , CM000672.2:g.99844215_99844217del	GRCh38
NC_000010.10:g.101603972_101603974del , CM000672.1:g.101603972_101603974del	GRCh37
NC_000010.9:g.101593962_101593964del	NCBI36
NG_011798.1:g.66510_66512del
NG_011798.2:g.66618_66620del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3844-107_3844-105del MANE Select	ENSP00000497274.1:n.3844-107_3844-105del
ENST00000649459.1:n.192-107_192-105del
ENST00000370449.8:c.3844-107_3844-105del	ENSP00000359478.4:n.3844-107_3844-105del
NM_000392.4:c.3844-107_3844-105del	NP_000383.1:n.3844-107_3844-105del
XM_006717630.2:c.3148-107_3148-105del	XP_006717693.1:n.3148-107_3148-105del
XR_945604.1:n.4033-107_4033-105del
XR_945605.1:n.3908-107_3908-105del
NM_000392.5:c.3844-107_3844-105del MANE Select	NP_000383.2:n.3844-107_3844-105del
XM_006717630.3:c.3148-107_3148-105del	XP_006717693.1:n.3148-107_3148-105del
XR_945604.3:n.4087-107_4087-105del
XR_945605.3:n.3960-107_3960-105del