Canonical Allele Identifier: CA394882220

Gene: ABCC1

Linked Data

• MyVariant Identifiers: chr16:g.16110468T>C (hg19) ; chr16:g.16016611T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016611T>C , CM000678.2:g.16016611T>C	GRCh38
NC_000016.9:g.16110468T>C , CM000678.1:g.16110468T>C	GRCh37
NC_000016.8:g.16017969T>C	NCBI36
NG_028268.1:g.72035T>C
NG_028268.2:g.72035T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.605T>C	ENSP00000382340.4:p.Ile202Thr
ENST00000399410.8:c.605T>C MANE Select	ENSP00000382342.3:p.Ile202Thr
ENST00000572882.3:c.605T>C	ENSP00000461615.2:p.Ile202Thr
ENST00000574224.2:n.680T>C
ENST00000677164.1:c.489+1983T>C	ENSP00000502873.1:n.489+1983T>C
ENST00000678422.1:c.605T>C	ENSP00000503954.1:p.Ile202Thr
ENST00000679043.1:n.557T>C
ENST00000399408.6:c.-374T>C	ENSP00000382340.3:n.-374T>C
ENST00000399410.7:c.605T>C	ENSP00000382342.3:p.Ile202Thr
ENST00000572882.2:c.300T>C
ENST00000574224.1:n.205T>C
NM_004996.3:c.605T>C	NP_004987.2:p.Ile202Thr
XM_011522497.1:c.581T>C	XP_011520799.1:p.Ile194Thr
XM_011522498.1:c.659T>C	XP_011520800.1:p.Ile220Thr
XM_011522498.2:c.659T>C	XP_011520800.1:p.Ile220Thr
XM_017023237.1:c.659T>C	XP_016878726.1:p.Ile220Thr
XM_017023238.1:c.543+1983T>C	XP_016878727.1:n.543+1983T>C
XM_017023239.1:c.521T>C	XP_016878728.1:p.Ile174Thr
XM_017023240.1:c.659T>C	XP_016878729.1:p.Ile220Thr
XM_017023241.1:c.405+6710T>C	XP_016878730.1:n.405+6710T>C
XM_017023242.1:c.659T>C	XP_016878731.1:p.Ile220Thr
XM_017023243.2:c.659T>C	XP_016878732.1:p.Ile220Thr
NM_004996.4:c.605T>C MANE Select	NP_004987.2:p.Ile202Thr