Canonical Allele Identifier: CA2210143247

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169695C= , CM000678.2:g.16169695C=	GRCh38
NC_000016.9:g.16263552C= , CM000678.1:g.16263552C=	GRCh37
NC_000016.8:g.16171053C=	NCBI36
NG_007558.2:g.58777G=
NG_007558.3:g.58923G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2946G=	ENSP00000483331.2:p.Thr982=
ENST00000205557.12:c.2946G= MANE Select	ENSP00000205557.7:p.Thr982=
ENST00000205557.11:c.2946G=	ENSP00000205557.7:p.Thr982=
ENST00000456970.6:c.2771G=	ENSP00000405002.2:n.2771G=
ENST00000622290.4:c.*155G=	ENSP00000483331.1:n.*155G=
NM_001171.5:c.2946G=	NP_001162.4:p.Thr982=
XM_011522479.1:c.2913G=	XP_011520781.1:p.Thr971=
XM_011522480.1:c.2604G=	XP_011520782.1:p.Thr868=
XM_011522481.1:c.2604G=	XP_011520783.1:p.Thr868=
XR_932836.1:n.3181G=
XR_932837.1:n.3182G=
XR_932838.1:n.3182G=
NM_001351800.1:c.2604G=	NP_001338729.1:p.Thr868=
NR_147784.1:n.2808G=
XM_011522479.2:c.2913G=	XP_011520781.1:p.Thr971=
XM_011522481.3:c.2604G=	XP_011520783.1:p.Thr868=
XM_017023212.1:c.2778G=	XP_016878701.1:p.Thr926=
XM_017023214.1:c.2946G=	XP_016878703.1:p.Thr982=
XM_024450261.1:c.2982G=	XP_024306029.1:p.Thr994=
XR_932836.2:n.3127G=
XR_932837.3:n.3127G=
XR_932838.3:n.3127G=
NM_001171.6:c.2946G= MANE Select	NP_001162.5:p.Thr982=