Canonical Allele Identifier: CA1931511196

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99818534_99818536delinsTTG , CM000672.2:g.99818534_99818536delinsTTG	GRCh38
NC_000010.10:g.101578291_101578293delinsTTG , CM000672.1:g.101578291_101578293delinsTTG	GRCh37
NC_000010.9:g.101568281_101568283delinsTTG	NCBI36
NG_011798.1:g.40829_40831delinsTTG
NG_011798.2:g.40937_40939delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2272-256_2272-254delinsTTG MANE Select	ENSP00000497274.1:n.2272-256_2272-254delinsTTG
ENST00000370449.8:c.2272-256_2272-254delinsTTG	ENSP00000359478.4:n.2272-256_2272-254delinsTTG
NM_000392.4:c.2272-256_2272-254delinsTTG	NP_000383.1:n.2272-256_2272-254delinsTTG
XM_006717630.2:c.1576-256_1576-254delinsTTG	XP_006717693.1:n.1576-256_1576-254delinsTTG
XM_006717631.2:c.2272-256_2272-254delinsTTG	XP_006717694.1:n.2272-256_2272-254delinsTTG
XM_011539291.1:c.2272-256_2272-254delinsTTG	XP_011537593.1:n.2272-256_2272-254delinsTTG
XR_945604.1:n.2461-256_2461-254delinsTTG
XR_945605.1:n.2463-256_2463-254delinsTTG
NM_000392.5:c.2272-256_2272-254delinsTTG MANE Select	NP_000383.2:n.2272-256_2272-254delinsTTG
XM_006717630.3:c.1576-256_1576-254delinsTTG	XP_006717693.1:n.1576-256_1576-254delinsTTG
XM_006717631.4:c.2272-256_2272-254delinsTTG	XP_006717694.1:n.2272-256_2272-254delinsTTG
XM_011539291.3:c.2272-256_2272-254delinsTTG	XP_011537593.1:n.2272-256_2272-254delinsTTG
XM_017015675.2:c.2272-256_2272-254delinsTTG	XP_016871164.1:n.2272-256_2272-254delinsTTG
XR_945604.3:n.2515-256_2515-254delinsTTG
XR_945605.3:n.2515-256_2515-254delinsTTG