Canonical Allele Identifier: CA2210149748
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16182856A= , CM000678.2:g.16182856A= GRCh38
NC_000016.9:g.16276713A= , CM000678.1:g.16276713A= GRCh37
NC_000016.8:g.16184214A= NCBI36
NG_007558.2:g.45616T=
NG_007558.3:g.45762T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.2018T= ENSP00000483331.2:p.Leu673=
ENST00000205557.12:c.2018T= MANE Select ENSP00000205557.7:p.Leu673=
ENST00000205557.11:c.2018T= ENSP00000205557.7:p.Leu673=
ENST00000456970.6:c.2018T= ENSP00000405002.2:p.Leu673=
ENST00000574094.5:n.2040-931T=
ENST00000622290.4:c.2018T= ENSP00000483331.1:p.Leu673=
NM_001171.5:c.2018T= NP_001162.4:p.Leu673=
XM_011522479.1:c.2018T= XP_011520781.1:p.Leu673=
XM_011522480.1:c.1676T= XP_011520782.1:p.Leu559=
XM_011522481.1:c.1676T= XP_011520783.1:p.Leu559=
XM_011522482.1:c.2018T= XP_011520784.1:p.Leu673=
XR_932836.1:n.2253T=
XR_932837.1:n.2254T=
XR_932838.1:n.2254T=
NM_001351800.1:c.1676T= NP_001338729.1:p.Leu559=
NR_147784.1:n.2055T=
XM_011522479.2:c.2018T= XP_011520781.1:p.Leu673=
XM_011522481.3:c.1676T= XP_011520783.1:p.Leu559=
XM_011522482.3:c.2018T= XP_011520784.1:p.Leu673=
XM_017023212.1:c.2018T= XP_016878701.1:p.Leu673=
XM_017023214.1:c.2018T= XP_016878703.1:p.Leu673=
XM_024450261.1:c.2054T= XP_024306029.1:p.Leu685=
XR_932836.2:n.2199T=
XR_932837.3:n.2199T=
XR_932838.3:n.2199T=
NM_001171.6:c.2018T= MANE Select NP_001162.5:p.Leu673=