Canonical Allele Identifier: CA394882204

Gene: ABCC1

Linked Data

• MyVariant Identifiers: chr16:g.16110464A>C (hg19) ; chr16:g.16016607A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016607A>C , CM000678.2:g.16016607A>C	GRCh38
NC_000016.9:g.16110464A>C , CM000678.1:g.16110464A>C	GRCh37
NC_000016.8:g.16017965A>C	NCBI36
NG_028268.1:g.72031A>C
NG_028268.2:g.72031A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.601A>C	ENSP00000382340.4:p.Thr201Pro
ENST00000399410.8:c.601A>C MANE Select	ENSP00000382342.3:p.Thr201Pro
ENST00000572882.3:c.601A>C	ENSP00000461615.2:p.Thr201Pro
ENST00000574224.2:n.676A>C
ENST00000677164.1:c.489+1979A>C	ENSP00000502873.1:n.489+1979A>C
ENST00000678422.1:c.601A>C	ENSP00000503954.1:p.Thr201Pro
ENST00000679043.1:n.553A>C
ENST00000399408.6:c.-378A>C	ENSP00000382340.3:n.-378A>C
ENST00000399410.7:c.601A>C	ENSP00000382342.3:p.Thr201Pro
ENST00000572882.2:c.296A>C
ENST00000574224.1:n.201A>C
NM_004996.3:c.601A>C	NP_004987.2:p.Thr201Pro
XM_011522497.1:c.577A>C	XP_011520799.1:p.Thr193Pro
XM_011522498.1:c.655A>C	XP_011520800.1:p.Thr219Pro
XM_011522498.2:c.655A>C	XP_011520800.1:p.Thr219Pro
XM_017023237.1:c.655A>C	XP_016878726.1:p.Thr219Pro
XM_017023238.1:c.543+1979A>C	XP_016878727.1:n.543+1979A>C
XM_017023239.1:c.517A>C	XP_016878728.1:p.Thr173Pro
XM_017023240.1:c.655A>C	XP_016878729.1:p.Thr219Pro
XM_017023241.1:c.405+6706A>C	XP_016878730.1:n.405+6706A>C
XM_017023242.1:c.655A>C	XP_016878731.1:p.Thr219Pro
XM_017023243.2:c.655A>C	XP_016878732.1:p.Thr219Pro
NM_004996.4:c.601A>C MANE Select	NP_004987.2:p.Thr201Pro