Canonical Allele Identifier: CA1931489602

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830589_99830591delinsTTG , CM000672.2:g.99830589_99830591delinsTTG	GRCh38
NC_000010.10:g.101590346_101590348delinsTTG , CM000672.1:g.101590346_101590348delinsTTG	GRCh37
NC_000010.9:g.101580336_101580338delinsTTG	NCBI36
NG_011798.1:g.52884_52886delinsTTG
NG_011798.2:g.52992_52994delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2748-127_2748-125delinsTTG MANE Select	ENSP00000497274.1:n.2748-127_2748-125delinsTTG
ENST00000370449.8:c.2748-127_2748-125delinsTTG	ENSP00000359478.4:n.2748-127_2748-125delinsTTG
NM_000392.4:c.2748-127_2748-125delinsTTG	NP_000383.1:n.2748-127_2748-125delinsTTG
XM_006717630.2:c.2052-127_2052-125delinsTTG	XP_006717693.1:n.2052-127_2052-125delinsTTG
XM_011539291.1:c.2747+156_2747+158delinsTTG	XP_011537593.1:n.2747+156_2747+158delinsTTG
XR_945604.1:n.2937-127_2937-125delinsTTG
XR_945605.1:n.2939-127_2939-125delinsTTG
NM_000392.5:c.2748-127_2748-125delinsTTG MANE Select	NP_000383.2:n.2748-127_2748-125delinsTTG
XM_006717630.3:c.2052-127_2052-125delinsTTG	XP_006717693.1:n.2052-127_2052-125delinsTTG
XM_011539291.3:c.2747+156_2747+158delinsTTG	XP_011537593.1:n.2747+156_2747+158delinsTTG
XR_945604.3:n.2991-127_2991-125delinsTTG
XR_945605.3:n.2991-127_2991-125delinsTTG