Canonical Allele Identifier: CA2581253010

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15992976C>G , CM000678.2:g.15992976C>G	GRCh38
NC_000016.9:g.16086833C>G , CM000678.1:g.16086833C>G	GRCh37
NC_000016.8:g.15994334C>G	NCBI36
NG_028268.1:g.48400C>G
NG_028268.2:g.48400C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004996.4:c.49-14840C>G MANE Select	NP_004987.2:n.49-14840C>G
ENST00000399410.8:c.49-14840C>G MANE Select	ENSP00000382342.3:n.49-14840C>G
NM_004996.3:c.49-14840C>G	NP_004987.2:n.49-14840C>G
ENST00000399408.6:c.-930-14840C>G	ENSP00000382340.3:n.-930-14840C>G
ENST00000399408.7:c.49-14840C>G	ENSP00000382340.4:n.49-14840C>G
ENST00000399410.7:c.49-14840C>G	ENSP00000382342.3:n.49-14840C>G
ENST00000572882.3:c.49-14840C>G	ENSP00000461615.2:n.49-14840C>G
ENST00000574224.2:n.124-14840C>G
ENST00000677164.1:c.49-14840C>G	ENSP00000502873.1:n.49-14840C>G
ENST00000678422.1:c.49-14840C>G	ENSP00000503954.1:n.49-14840C>G
XM_011522498.1:c.102+724C>G	XP_011520800.1:n.102+724C>G
XM_011522498.2:c.102+724C>G	XP_011520800.1:n.102+724C>G
XM_017023237.1:c.102+724C>G	XP_016878726.1:n.102+724C>G
XM_017023238.1:c.102+724C>G	XP_016878727.1:n.102+724C>G
XM_017023239.1:c.102+724C>G	XP_016878728.1:n.102+724C>G
XM_017023240.1:c.102+724C>G	XP_016878729.1:n.102+724C>G
XM_017023241.1:c.102+724C>G	XP_016878730.1:n.102+724C>G
XM_017023242.1:c.102+724C>G	XP_016878731.1:n.102+724C>G
XM_017023243.2:c.102+724C>G	XP_016878732.1:n.102+724C>G