Canonical Allele Identifier: CA1931509394

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99817381_99817383delinsCAG , CM000672.2:g.99817381_99817383delinsCAG	GRCh38
NC_000010.10:g.101577138_101577140delinsCAG , CM000672.1:g.101577138_101577140delinsCAG	GRCh37
NC_000010.9:g.101567128_101567130delinsCAG	NCBI36
NG_011798.1:g.39676_39678delinsCAG
NG_011798.2:g.39784_39786delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2168_2170delinsCAG MANE Select	ENSP00000497274.1:p.Thr723=
ENST00000370449.8:c.2168_2170delinsCAG	ENSP00000359478.4:p.Thr723=
NM_000392.4:c.2168_2170delinsCAG	NP_000383.1:p.Thr723=
XM_006717630.2:c.1472_1474delinsCAG	XP_006717693.1:p.Thr491=
XM_006717631.2:c.2168_2170delinsCAG	XP_006717694.1:p.Thr723=
XM_011539291.1:c.2168_2170delinsCAG	XP_011537593.1:p.Thr723=
XR_945604.1:n.2357_2359delinsCAG
XR_945605.1:n.2359_2361delinsCAG
NM_000392.5:c.2168_2170delinsCAG MANE Select	NP_000383.2:p.Thr723=
XM_006717630.3:c.1472_1474delinsCAG	XP_006717693.1:p.Thr491=
XM_006717631.4:c.2168_2170delinsCAG	XP_006717694.1:p.Thr723=
XM_011539291.3:c.2168_2170delinsCAG	XP_011537593.1:p.Thr723=
XM_017015675.2:c.2168_2170delinsCAG	XP_016871164.1:p.Thr723=
XR_945604.3:n.2411_2413delinsCAG
XR_945605.3:n.2411_2413delinsCAG