Canonical Allele Identifier: CA2210140659

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154788T= , CM000678.2:g.16154788T=	GRCh38
NC_000016.9:g.16248645T= , CM000678.1:g.16248645T=	GRCh37
NC_000016.8:g.16156146T=	NCBI36
NG_007558.2:g.73684A=
NG_007558.3:g.73830A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.911A=
ENST00000622290.5:c.*220A=	ENSP00000483331.2:n.*220A=
ENST00000205557.12:c.4048A= MANE Select	ENSP00000205557.7:p.Ile1350=
ENST00000640696.1:c.862A=	ENSP00000492197.1:p.Ile288=
ENST00000205557.11:c.4048A=	ENSP00000205557.7:p.Ile1350=
ENST00000456970.6:c.3673A=	ENSP00000405002.2:n.3673A=
ENST00000576204.5:n.911A=
ENST00000622290.4:c.*1257A=	ENSP00000483331.1:n.*1257A=
NM_001171.5:c.4048A=	NP_001162.4:p.Ile1350=
XM_011522479.1:c.4015A=	XP_011520781.1:p.Ile1339=
XM_011522480.1:c.3706A=	XP_011520782.1:p.Ile1236=
XM_011522481.1:c.3706A=	XP_011520783.1:p.Ile1236=
XR_933134.1:n.539-4993T=
NM_001351800.1:c.3706A=	NP_001338729.1:p.Ile1236=
NR_147784.1:n.3710A=
XM_011522479.2:c.4015A=	XP_011520781.1:p.Ile1339=
XM_011522481.3:c.3706A=	XP_011520783.1:p.Ile1236=
XM_017023212.1:c.3880A=	XP_016878701.1:p.Ile1294=
XM_024450261.1:c.4084A=	XP_024306029.1:p.Ile1362=
NM_001171.6:c.4048A= MANE Select	NP_001162.5:p.Ile1350=