Canonical Allele Identifier: CA1931511686

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844155_99844156delinsAG , CM000672.2:g.99844155_99844156delinsAG	GRCh38
NC_000010.10:g.101603912_101603913delinsAG , CM000672.1:g.101603912_101603913delinsAG	GRCh37
NC_000010.9:g.101593902_101593903delinsAG	NCBI36
NG_011798.1:g.66450_66451delinsAG
NG_011798.2:g.66558_66559delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3844-167_3844-166delinsAG MANE Select	ENSP00000497274.1:n.3844-167_3844-166delinsAG
ENST00000649459.1:n.192-167_192-166delinsAG
ENST00000370449.8:c.3844-167_3844-166delinsAG	ENSP00000359478.4:n.3844-167_3844-166delinsAG
NM_000392.4:c.3844-167_3844-166delinsAG	NP_000383.1:n.3844-167_3844-166delinsAG
XM_006717630.2:c.3148-167_3148-166delinsAG	XP_006717693.1:n.3148-167_3148-166delinsAG
XR_945604.1:n.4033-167_4033-166delinsAG
XR_945605.1:n.3908-167_3908-166delinsAG
NM_000392.5:c.3844-167_3844-166delinsAG MANE Select	NP_000383.2:n.3844-167_3844-166delinsAG
XM_006717630.3:c.3148-167_3148-166delinsAG	XP_006717693.1:n.3148-167_3148-166delinsAG
XR_945604.3:n.4087-167_4087-166delinsAG
XR_945605.3:n.3960-167_3960-166delinsAG