Canonical Allele Identifier: CA2843473553

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99817419dup , CM000672.2:g.99817419dup	GRCh38
NC_000010.10:g.101577176dup , CM000672.1:g.101577176dup	GRCh37
NC_000010.9:g.101567166dup	NCBI36
NG_011798.1:g.39714dup
NG_011798.2:g.39822dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2206dup MANE Select	ENSP00000497274.1:p.Ala736GlyfsTer18
ENST00000370449.8:c.2206dup	ENSP00000359478.4:p.Ala736GlyfsTer18
NM_000392.4:c.2206dup	NP_000383.1:p.Ala736GlyfsTer18
XM_006717630.2:c.1510dup	XP_006717693.1:p.Ala504GlyfsTer18
XM_006717631.2:c.2206dup	XP_006717694.1:p.Ala736GlyfsTer18
XM_011539291.1:c.2206dup	XP_011537593.1:p.Ala736GlyfsTer18
XR_945604.1:n.2395dup
XR_945605.1:n.2397dup
NM_000392.5:c.2206dup MANE Select	NP_000383.2:p.Ala736GlyfsTer18
XM_006717630.3:c.1510dup	XP_006717693.1:p.Ala504GlyfsTer18
XM_006717631.4:c.2206dup	XP_006717694.1:p.Ala736GlyfsTer18
XM_011539291.3:c.2206dup	XP_011537593.1:p.Ala736GlyfsTer18
XM_017015675.2:c.2206dup	XP_016871164.1:p.Ala736GlyfsTer18
XR_945604.3:n.2449dup
XR_945605.3:n.2449dup