Canonical Allele Identifier: CA1931511690

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844160_99844161delinsCT , CM000672.2:g.99844160_99844161delinsCT	GRCh38
NC_000010.10:g.101603917_101603918delinsCT , CM000672.1:g.101603917_101603918delinsCT	GRCh37
NC_000010.9:g.101593907_101593908delinsCT	NCBI36
NG_011798.1:g.66455_66456delinsCT
NG_011798.2:g.66563_66564delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3844-162_3844-161delinsCT MANE Select	ENSP00000497274.1:n.3844-162_3844-161delinsCT
ENST00000649459.1:n.192-162_192-161delinsCT
ENST00000370449.8:c.3844-162_3844-161delinsCT	ENSP00000359478.4:n.3844-162_3844-161delinsCT
NM_000392.4:c.3844-162_3844-161delinsCT	NP_000383.1:n.3844-162_3844-161delinsCT
XM_006717630.2:c.3148-162_3148-161delinsCT	XP_006717693.1:n.3148-162_3148-161delinsCT
XR_945604.1:n.4033-162_4033-161delinsCT
XR_945605.1:n.3908-162_3908-161delinsCT
NM_000392.5:c.3844-162_3844-161delinsCT MANE Select	NP_000383.2:n.3844-162_3844-161delinsCT
XM_006717630.3:c.3148-162_3148-161delinsCT	XP_006717693.1:n.3148-162_3148-161delinsCT
XR_945604.3:n.4087-162_4087-161delinsCT
XR_945605.3:n.3960-162_3960-161delinsCT