Canonical Allele Identifier: CA394882022

Gene: ABCC1

Linked Data

• MyVariant Identifiers: chr16:g.16110378A>C (hg19) ; chr16:g.16016521A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016521A>C , CM000678.2:g.16016521A>C	GRCh38
NC_000016.9:g.16110378A>C , CM000678.1:g.16110378A>C	GRCh37
NC_000016.8:g.16017879A>C	NCBI36
NG_028268.1:g.71945A>C
NG_028268.2:g.71945A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.515A>C	ENSP00000382340.4:p.Asp172Ala
ENST00000399410.8:c.515A>C MANE Select	ENSP00000382342.3:p.Asp172Ala
ENST00000572882.3:c.515A>C	ENSP00000461615.2:p.Asp172Ala
ENST00000574224.2:n.590A>C
ENST00000677164.1:c.489+1893A>C	ENSP00000502873.1:n.489+1893A>C
ENST00000678422.1:c.515A>C	ENSP00000503954.1:p.Asp172Ala
ENST00000679043.1:n.467A>C
ENST00000399408.6:c.-464A>C	ENSP00000382340.3:n.-464A>C
ENST00000399410.7:c.515A>C	ENSP00000382342.3:p.Asp172Ala
ENST00000572882.2:c.210A>C
ENST00000574224.1:n.115A>C
NM_004996.3:c.515A>C	NP_004987.2:p.Asp172Ala
XM_011522497.1:c.491A>C	XP_011520799.1:p.Asp164Ala
XM_011522498.1:c.569A>C	XP_011520800.1:p.Asp190Ala
XM_011522498.2:c.569A>C	XP_011520800.1:p.Asp190Ala
XM_017023237.1:c.569A>C	XP_016878726.1:p.Asp190Ala
XM_017023238.1:c.543+1893A>C	XP_016878727.1:n.543+1893A>C
XM_017023239.1:c.431A>C	XP_016878728.1:p.Asp144Ala
XM_017023240.1:c.569A>C	XP_016878729.1:p.Asp190Ala
XM_017023241.1:c.405+6620A>C	XP_016878730.1:n.405+6620A>C
XM_017023242.1:c.569A>C	XP_016878731.1:p.Asp190Ala
XM_017023243.2:c.569A>C	XP_016878732.1:p.Asp190Ala
NM_004996.4:c.515A>C MANE Select	NP_004987.2:p.Asp172Ala