Canonical Allele Identifier: CA394882005

Gene: ABCC1

Linked Data

• MyVariant Identifiers: chr16:g.16110368C>G (hg19) ; chr16:g.16016511C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016511C>G , CM000678.2:g.16016511C>G	GRCh38
NC_000016.9:g.16110368C>G , CM000678.1:g.16110368C>G	GRCh37
NC_000016.8:g.16017869C>G	NCBI36
NG_028268.1:g.71935C>G
NG_028268.2:g.71935C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.505C>G	ENSP00000382340.4:p.Leu169Val
ENST00000399410.8:c.505C>G MANE Select	ENSP00000382342.3:p.Leu169Val
ENST00000572882.3:c.505C>G	ENSP00000461615.2:p.Leu169Val
ENST00000574224.2:n.580C>G
ENST00000677164.1:c.489+1883C>G	ENSP00000502873.1:n.489+1883C>G
ENST00000678422.1:c.505C>G	ENSP00000503954.1:p.Leu169Val
ENST00000679043.1:n.457C>G
ENST00000399408.6:c.-474C>G	ENSP00000382340.3:n.-474C>G
ENST00000399410.7:c.505C>G	ENSP00000382342.3:p.Leu169Val
ENST00000572882.2:c.200C>G
ENST00000574224.1:n.105C>G
NM_004996.3:c.505C>G	NP_004987.2:p.Leu169Val
XM_011522497.1:c.481C>G	XP_011520799.1:p.Leu161Val
XM_011522498.1:c.559C>G	XP_011520800.1:p.Leu187Val
XM_011522498.2:c.559C>G	XP_011520800.1:p.Leu187Val
XM_017023237.1:c.559C>G	XP_016878726.1:p.Leu187Val
XM_017023238.1:c.543+1883C>G	XP_016878727.1:n.543+1883C>G
XM_017023239.1:c.421C>G	XP_016878728.1:p.Leu141Val
XM_017023240.1:c.559C>G	XP_016878729.1:p.Leu187Val
XM_017023241.1:c.405+6610C>G	XP_016878730.1:n.405+6610C>G
XM_017023242.1:c.559C>G	XP_016878731.1:p.Leu187Val
XM_017023243.2:c.559C>G	XP_016878732.1:p.Leu187Val
NM_004996.4:c.505C>G MANE Select	NP_004987.2:p.Leu169Val