Canonical Allele Identifier: CA493794541
Gene: ABCC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.16110364G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16016507G>A , CM000678.2:g.16016507G>A GRCh38
NC_000016.9:g.16110364G>A , CM000678.1:g.16110364G>A GRCh37
NC_000016.8:g.16017865G>A NCBI36
NG_028268.1:g.71931G>A
NG_028268.2:g.71931G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399408.7:c.501G>A ENSP00000382340.4:p.Val167=
ENST00000399410.8:c.501G>A MANE Select ENSP00000382342.3:p.Val167=
ENST00000572882.3:c.501G>A ENSP00000461615.2:p.Val167=
ENST00000574224.2:n.576G>A
ENST00000677164.1:c.489+1879G>A ENSP00000502873.1:n.489+1879G>A
ENST00000678422.1:c.501G>A ENSP00000503954.1:p.Val167=
ENST00000679043.1:n.453G>A
ENST00000399408.6:c.-478G>A ENSP00000382340.3:n.-478G>A
ENST00000399410.7:c.501G>A ENSP00000382342.3:p.Val167=
ENST00000572882.2:c.196G>A
ENST00000574224.1:n.101G>A
NM_004996.3:c.501G>A NP_004987.2:p.Val167=
XM_011522497.1:c.477G>A XP_011520799.1:p.Val159=
XM_011522498.1:c.555G>A XP_011520800.1:p.Val185=
XM_011522498.2:c.555G>A XP_011520800.1:p.Val185=
XM_017023237.1:c.555G>A XP_016878726.1:p.Val185=
XM_017023238.1:c.543+1879G>A XP_016878727.1:n.543+1879G>A
XM_017023239.1:c.417G>A XP_016878728.1:p.Val139=
XM_017023240.1:c.555G>A XP_016878729.1:p.Val185=
XM_017023241.1:c.405+6606G>A XP_016878730.1:n.405+6606G>A
XM_017023242.1:c.555G>A XP_016878731.1:p.Val185=
XM_017023243.2:c.555G>A XP_016878732.1:p.Val185=
NM_004996.4:c.501G>A MANE Select NP_004987.2:p.Val167=