Canonical Allele Identifier: CA2210143256

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169712C= , CM000678.2:g.16169712C=	GRCh38
NC_000016.9:g.16263569C= , CM000678.1:g.16263569C=	GRCh37
NC_000016.8:g.16171070C=	NCBI36
NG_007558.2:g.58760G=
NG_007558.3:g.58906G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2929G=	ENSP00000483331.2:p.Val977=
ENST00000205557.12:c.2929G= MANE Select	ENSP00000205557.7:p.Val977=
ENST00000205557.11:c.2929G=	ENSP00000205557.7:p.Val977=
ENST00000456970.6:c.2754G=	ENSP00000405002.2:n.2754G=
ENST00000622290.4:c.*138G=	ENSP00000483331.1:n.*138G=
NM_001171.5:c.2929G=	NP_001162.4:p.Val977=
XM_011522479.1:c.2896G=	XP_011520781.1:p.Val966=
XM_011522480.1:c.2587G=	XP_011520782.1:p.Val863=
XM_011522481.1:c.2587G=	XP_011520783.1:p.Val863=
XR_932836.1:n.3164G=
XR_932837.1:n.3165G=
XR_932838.1:n.3165G=
NM_001351800.1:c.2587G=	NP_001338729.1:p.Val863=
NR_147784.1:n.2791G=
XM_011522479.2:c.2896G=	XP_011520781.1:p.Val966=
XM_011522481.3:c.2587G=	XP_011520783.1:p.Val863=
XM_017023212.1:c.2761G=	XP_016878701.1:p.Val921=
XM_017023214.1:c.2929G=	XP_016878703.1:p.Val977=
XM_024450261.1:c.2965G=	XP_024306029.1:p.Val989=
XR_932836.2:n.3110G=
XR_932837.3:n.3110G=
XR_932838.3:n.3110G=
NM_001171.6:c.2929G= MANE Select	NP_001162.5:p.Val977=