Canonical Allele Identifier: CA2610497811

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99844613-ACACAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844614_99844618del , CM000672.2:g.99844614_99844618del	GRCh38
NC_000010.10:g.101604371_101604375del , CM000672.1:g.101604371_101604375del	GRCh37
NC_000010.9:g.101594361_101594365del	NCBI36
NG_011798.1:g.66909_66913del
NG_011798.2:g.67017_67021del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3987+149_3987+153del MANE Select	ENSP00000497274.1:n.3987+149_3987+153del
ENST00000649459.1:n.335+149_335+153del
ENST00000370449.8:c.3987+149_3987+153del	ENSP00000359478.4:n.3987+149_3987+153del
NM_000392.4:c.3987+149_3987+153del	NP_000383.1:n.3987+149_3987+153del
XM_006717630.2:c.3291+149_3291+153del	XP_006717693.1:n.3291+149_3291+153del
XR_945604.1:n.4176+149_4176+153del
XR_945605.1:n.4051+149_4051+153del
NM_000392.5:c.3987+149_3987+153del MANE Select	NP_000383.2:n.3987+149_3987+153del
XM_006717630.3:c.3291+149_3291+153del	XP_006717693.1:n.3291+149_3291+153del
XR_945604.3:n.4230+149_4230+153del
XR_945605.3:n.4103+149_4103+153del