Canonical Allele Identifier: CA2610497722

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99844351-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844353del , CM000672.2:g.99844353del	GRCh38
NC_000010.10:g.101604110del , CM000672.1:g.101604110del	GRCh37
NC_000010.9:g.101594100del	NCBI36
NG_011798.1:g.66648del
NG_011798.2:g.66756del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3875del MANE Select	ENSP00000497274.1:p.Pro1292GlnfsTer?
ENST00000649459.1:n.223del
ENST00000370449.8:c.3875del	ENSP00000359478.4:p.Pro1292GlnfsTer?
NM_000392.4:c.3875del	NP_000383.1:p.Pro1292GlnfsTer?
XM_006717630.2:c.3179del	XP_006717693.1:p.Pro1060GlnfsTer?
XR_945604.1:n.4064del
XR_945605.1:n.3939del
NM_000392.5:c.3875del MANE Select	NP_000383.2:p.Pro1292GlnfsTer?
XM_006717630.3:c.3179del	XP_006717693.1:p.Pro1060GlnfsTer?
XR_945604.3:n.4118del
XR_945605.3:n.3991del