Canonical Allele Identifier: CA1931489422

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830492_99830493delinsTC , CM000672.2:g.99830492_99830493delinsTC	GRCh38
NC_000010.10:g.101590249_101590250delinsTC , CM000672.1:g.101590249_101590250delinsTC	GRCh37
NC_000010.9:g.101580239_101580240delinsTC	NCBI36
NG_011798.1:g.52787_52788delinsTC
NG_011798.2:g.52895_52896delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2747+59_2747+60delinsTC MANE Select	ENSP00000497274.1:n.2747+59_2747+60delinsTC
ENST00000370449.8:c.2747+59_2747+60delinsTC	ENSP00000359478.4:n.2747+59_2747+60delinsTC
NM_000392.4:c.2747+59_2747+60delinsTC	NP_000383.1:n.2747+59_2747+60delinsTC
XM_006717630.2:c.2051+59_2051+60delinsTC	XP_006717693.1:n.2051+59_2051+60delinsTC
XM_011539291.1:c.2747+59_2747+60delinsTC	XP_011537593.1:n.2747+59_2747+60delinsTC
XR_945604.1:n.2936+59_2936+60delinsTC
XR_945605.1:n.2938+59_2938+60delinsTC
NM_000392.5:c.2747+59_2747+60delinsTC MANE Select	NP_000383.2:n.2747+59_2747+60delinsTC
XM_006717630.3:c.2051+59_2051+60delinsTC	XP_006717693.1:n.2051+59_2051+60delinsTC
XM_011539291.3:c.2747+59_2747+60delinsTC	XP_011537593.1:n.2747+59_2747+60delinsTC
XR_945604.3:n.2990+59_2990+60delinsTC
XR_945605.3:n.2990+59_2990+60delinsTC