Canonical Allele Identifier: CA394882045

Gene: ABCC1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016532T>A , CM000678.2:g.16016532T>A	GRCh38
NC_000016.9:g.16110389T>A , CM000678.1:g.16110389T>A	GRCh37
NC_000016.8:g.16017890T>A	NCBI36
NG_028268.1:g.71956T>A
NG_028268.2:g.71956T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.526T>A	ENSP00000382340.4:p.Tyr176Asn
ENST00000399410.8:c.526T>A MANE Select	ENSP00000382342.3:p.Tyr176Asn
ENST00000572882.3:c.526T>A	ENSP00000461615.2:p.Tyr176Asn
ENST00000574224.2:n.601T>A
ENST00000677164.1:c.489+1904T>A	ENSP00000502873.1:n.489+1904T>A
ENST00000678422.1:c.526T>A	ENSP00000503954.1:p.Tyr176Asn
ENST00000679043.1:n.478T>A
ENST00000399408.6:c.-453T>A	ENSP00000382340.3:n.-453T>A
ENST00000399410.7:c.526T>A	ENSP00000382342.3:p.Tyr176Asn
ENST00000572882.2:c.221T>A
ENST00000574224.1:n.126T>A
NM_004996.3:c.526T>A	NP_004987.2:p.Tyr176Asn
XM_011522497.1:c.502T>A	XP_011520799.1:p.Tyr168Asn
XM_011522498.1:c.580T>A	XP_011520800.1:p.Tyr194Asn
XM_011522498.2:c.580T>A	XP_011520800.1:p.Tyr194Asn
XM_017023237.1:c.580T>A	XP_016878726.1:p.Tyr194Asn
XM_017023238.1:c.543+1904T>A	XP_016878727.1:n.543+1904T>A
XM_017023239.1:c.442T>A	XP_016878728.1:p.Tyr148Asn
XM_017023240.1:c.580T>A	XP_016878729.1:p.Tyr194Asn
XM_017023241.1:c.405+6631T>A	XP_016878730.1:n.405+6631T>A
XM_017023242.1:c.580T>A	XP_016878731.1:p.Tyr194Asn
XM_017023243.2:c.580T>A	XP_016878732.1:p.Tyr194Asn
NM_004996.4:c.526T>A MANE Select	NP_004987.2:p.Tyr176Asn