Canonical Allele Identifier: CA2210137173

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16163249T= , CM000678.2:g.16163249T=	GRCh38
NC_000016.9:g.16257106T= , CM000678.1:g.16257106T=	GRCh37
NC_000016.8:g.16164607T=	NCBI36
NG_007558.2:g.65223A=
NG_007558.3:g.65369A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3307-57A=	ENSP00000483331.2:n.3307-57A=
ENST00000205557.12:c.3307-57A= MANE Select	ENSP00000205557.7:n.3307-57A=
ENST00000640696.1:c.321-1685A=	ENSP00000492197.1:n.321-1685A=
ENST00000205557.11:c.3307-57A=	ENSP00000205557.7:n.3307-57A=
ENST00000456970.6:c.3132-1685A=	ENSP00000405002.2:n.3132-1685A=
ENST00000622290.4:c.*516-57A=	ENSP00000483331.1:n.*516-57A=
NM_001171.5:c.3307-57A=	NP_001162.4:n.3307-57A=
XM_011522479.1:c.3274-57A=	XP_011520781.1:n.3274-57A=
XM_011522480.1:c.2965-57A=	XP_011520782.1:n.2965-57A=
XM_011522481.1:c.2965-57A=	XP_011520783.1:n.2965-57A=
XR_932836.1:n.3542-57A=
XR_932837.1:n.3543-1685A=
XR_932838.1:n.3543-1685A=
XR_933133.1:n.407+406T=
XR_933134.1:n.754+406T=
NM_001351800.1:c.2965-57A=	NP_001338729.1:n.2965-57A=
NR_147784.1:n.3169-1685A=
XM_011522479.2:c.3274-57A=	XP_011520781.1:n.3274-57A=
XM_011522481.3:c.2965-57A=	XP_011520783.1:n.2965-57A=
XM_017023212.1:c.3139-57A=	XP_016878701.1:n.3139-57A=
XM_017023214.1:c.3307-1685A=	XP_016878703.1:n.3307-1685A=
XM_024450261.1:c.3343-57A=	XP_024306029.1:n.3343-57A=
XR_932836.2:n.3488-57A=
XR_932837.3:n.3488-1685A=
XR_932838.3:n.3488-1685A=
NM_001171.6:c.3307-57A= MANE Select	NP_001162.5:n.3307-57A=