Canonical Allele Identifier: CA2210125619

Gene: ABCC1

Linked Data

• dbSNP Id: rs2046152333

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16142309_16142324dup , CM000678.2:g.16142309_16142324dup	GRCh38
NC_000016.9:g.16236166_16236181dup , CM000678.1:g.16236166_16236181dup	GRCh37
NC_000016.8:g.16143667_16143682dup	NCBI36
NG_028268.1:g.197733_197748dup
NG_028268.2:g.197733_197748dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.*1028_*1043dup	ENSP00000382340.4:n.*1028_*1043dup
ENST00000399410.8:c.*1028_*1043dup MANE Select	ENSP00000382342.3:n.*1028_*1043dup
ENST00000572882.3:c.*1028_*1043dup	ENSP00000461615.2:n.*1028_*1043dup
ENST00000676806.1:n.2350_2365dup
ENST00000677164.1:c.*1028_*1043dup	ENSP00000502873.1:n.*1028_*1043dup
ENST00000678422.1:c.*2721_*2736dup	ENSP00000503954.1:n.*2721_*2736dup
ENST00000399408.6:c.*1028_*1043dup	ENSP00000382340.3:n.*1028_*1043dup
ENST00000399410.7:c.*1028_*1043dup	ENSP00000382342.3:n.*1028_*1043dup
NM_004996.3:c.*1028_*1043dup	NP_004987.2:n.*1028_*1043dup
XM_011522497.1:c.*1028_*1043dup	XP_011520799.1:n.*1028_*1043dup
XM_011522498.1:c.*1028_*1043dup	XP_011520800.1:n.*1028_*1043dup
XM_011522498.2:c.*1028_*1043dup	XP_011520800.1:n.*1028_*1043dup
XM_017023237.1:c.*1028_*1043dup	XP_016878726.1:n.*1028_*1043dup
XM_017023238.1:c.*1028_*1043dup	XP_016878727.1:n.*1028_*1043dup
XM_017023239.1:c.*1028_*1043dup	XP_016878728.1:n.*1028_*1043dup
XM_017023240.1:c.*1028_*1043dup	XP_016878729.1:n.*1028_*1043dup
XM_017023241.1:c.*1028_*1043dup	XP_016878730.1:n.*1028_*1043dup
XM_017023242.1:c.*1028_*1043dup	XP_016878731.1:n.*1028_*1043dup
NM_004996.4:c.*1028_*1043dup MANE Select	NP_004987.2:n.*1028_*1043dup