Canonical Allele Identifier: CA1931489661
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99830639_99830643delinsCTGAG , CM000672.2:g.99830639_99830643delinsCTGAG GRCh38
NC_000010.10:g.101590396_101590400delinsCTGAG , CM000672.1:g.101590396_101590400delinsCTGAG GRCh37
NC_000010.9:g.101580386_101580390delinsCTGAG NCBI36
NG_011798.1:g.52934_52938delinsCTGAG
NG_011798.2:g.53042_53046delinsCTGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.2748-77_2748-73delinsCTGAG MANE Select ENSP00000497274.1:n.2748-77_2748-73delinsCTGAG
ENST00000370449.8:c.2748-77_2748-73delinsCTGAG ENSP00000359478.4:n.2748-77_2748-73delinsCTGAG
NM_000392.4:c.2748-77_2748-73delinsCTGAG NP_000383.1:n.2748-77_2748-73delinsCTGAG
XM_006717630.2:c.2052-77_2052-73delinsCTGAG XP_006717693.1:n.2052-77_2052-73delinsCTGAG
XM_011539291.1:c.2747+206_2747+210delinsCTGAG XP_011537593.1:n.2747+206_2747+210delinsCTGAG
XR_945604.1:n.2937-77_2937-73delinsCTGAG
XR_945605.1:n.2939-77_2939-73delinsCTGAG
NM_000392.5:c.2748-77_2748-73delinsCTGAG MANE Select NP_000383.2:n.2748-77_2748-73delinsCTGAG
XM_006717630.3:c.2052-77_2052-73delinsCTGAG XP_006717693.1:n.2052-77_2052-73delinsCTGAG
XM_011539291.3:c.2747+206_2747+210delinsCTGAG XP_011537593.1:n.2747+206_2747+210delinsCTGAG
XR_945604.3:n.2991-77_2991-73delinsCTGAG
XR_945605.3:n.2991-77_2991-73delinsCTGAG