Canonical Allele Identifier: CA2210147942

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16178916G= , CM000678.2:g.16178916G=	GRCh38
NC_000016.9:g.16272773G= , CM000678.1:g.16272773G=	GRCh37
NC_000016.8:g.16180274G=	NCBI36
NG_007558.2:g.49556C=
NG_007558.3:g.49702C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001171.6:c.2297C= MANE Select	NP_001162.5:p.Ala766=
ENST00000205557.12:c.2297C= MANE Select	ENSP00000205557.7:p.Ala766=
NM_001171.5:c.2297C=	NP_001162.4:p.Ala766=
NM_001351800.1:c.1955C=	NP_001338729.1:p.Ala652=
NR_147784.1:n.2334C=
ENST00000205557.11:c.2297C=	ENSP00000205557.7:p.Ala766=
ENST00000456970.6:c.2297C=	ENSP00000405002.2:p.Ala766=
ENST00000622290.4:c.2297C=	ENSP00000483331.1:p.Ala766=
ENST00000622290.5:c.2297C=	ENSP00000483331.2:p.Ala766=
XM_011522479.1:c.2297C=	XP_011520781.1:p.Ala766=
XM_011522479.2:c.2297C=	XP_011520781.1:p.Ala766=
XM_011522480.1:c.1955C=	XP_011520782.1:p.Ala652=
XM_011522481.1:c.1955C=	XP_011520783.1:p.Ala652=
XM_011522481.3:c.1955C=	XP_011520783.1:p.Ala652=
XM_011522482.1:c.2297C=	XP_011520784.1:p.Ala766=
XM_011522482.3:c.2297C=	XP_011520784.1:p.Ala766=
XM_017023212.1:c.2248-1290C=	XP_016878701.1:n.2248-1290C=
XM_017023214.1:c.2297C=	XP_016878703.1:p.Ala766=
XM_024450261.1:c.2333C=	XP_024306029.1:p.Ala778=
XR_932836.1:n.2532C=
XR_932836.2:n.2478C=
XR_932837.1:n.2533C=
XR_932837.3:n.2478C=
XR_932838.1:n.2533C=
XR_932838.3:n.2478C=