Canonical Allele Identifier: CA1931512190

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844509_99844512delinsAAAC , CM000672.2:g.99844509_99844512delinsAAAC	GRCh38
NC_000010.10:g.101604266_101604269delinsAAAC , CM000672.1:g.101604266_101604269delinsAAAC	GRCh37
NC_000010.9:g.101594256_101594259delinsAAAC	NCBI36
NG_011798.1:g.66804_66807delinsAAAC
NG_011798.2:g.66912_66915delinsAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3987+44_3987+47delinsAAAC MANE Select	ENSP00000497274.1:n.3987+44_3987+47delinsAAAC
ENST00000649459.1:n.335+44_335+47delinsAAAC
ENST00000370449.8:c.3987+44_3987+47delinsAAAC	ENSP00000359478.4:n.3987+44_3987+47delinsAAAC
NM_000392.4:c.3987+44_3987+47delinsAAAC	NP_000383.1:n.3987+44_3987+47delinsAAAC
XM_006717630.2:c.3291+44_3291+47delinsAAAC	XP_006717693.1:n.3291+44_3291+47delinsAAAC
XR_945604.1:n.4176+44_4176+47delinsAAAC
XR_945605.1:n.4051+44_4051+47delinsAAAC
NM_000392.5:c.3987+44_3987+47delinsAAAC MANE Select	NP_000383.2:n.3987+44_3987+47delinsAAAC
XM_006717630.3:c.3291+44_3291+47delinsAAAC	XP_006717693.1:n.3291+44_3291+47delinsAAAC
XR_945604.3:n.4230+44_4230+47delinsAAAC
XR_945605.3:n.4103+44_4103+47delinsAAAC