Canonical Allele Identifier: CA1931489693

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830663_99830669delinsCAAGAAG , CM000672.2:g.99830663_99830669delinsCAAGAAG	GRCh38
NC_000010.10:g.101590420_101590426delinsCAAGAAG , CM000672.1:g.101590420_101590426delinsCAAGAAG	GRCh37
NC_000010.9:g.101580410_101580416delinsCAAGAAG	NCBI36
NG_011798.1:g.52958_52964delinsCAAGAAG
NG_011798.2:g.53066_53072delinsCAAGAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2748-53_2748-47delinsCAAGAAG MANE Select	ENSP00000497274.1:n.2748-53_2748-47delinsCAAGAAG
ENST00000370449.8:c.2748-53_2748-47delinsCAAGAAG	ENSP00000359478.4:n.2748-53_2748-47delinsCAAGAAG
NM_000392.4:c.2748-53_2748-47delinsCAAGAAG	NP_000383.1:n.2748-53_2748-47delinsCAAGAAG
XM_006717630.2:c.2052-53_2052-47delinsCAAGAAG	XP_006717693.1:n.2052-53_2052-47delinsCAAGAAG
XM_011539291.1:c.2747+230_2747+236delinsCAAGAAG	XP_011537593.1:n.2747+230_2747+236delinsCAAGAAG
XR_945604.1:n.2937-53_2937-47delinsCAAGAAG
XR_945605.1:n.2939-53_2939-47delinsCAAGAAG
NM_000392.5:c.2748-53_2748-47delinsCAAGAAG MANE Select	NP_000383.2:n.2748-53_2748-47delinsCAAGAAG
XM_006717630.3:c.2052-53_2052-47delinsCAAGAAG	XP_006717693.1:n.2052-53_2052-47delinsCAAGAAG
XM_011539291.3:c.2747+230_2747+236delinsCAAGAAG	XP_011537593.1:n.2747+230_2747+236delinsCAAGAAG
XR_945604.3:n.2991-53_2991-47delinsCAAGAAG
XR_945605.3:n.2991-53_2991-47delinsCAAGAAG