Canonical Allele Identifier: CA2210132132

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159616G= , CM000678.2:g.16159616G=	GRCh38
NC_000016.9:g.16253473G= , CM000678.1:g.16253473G=	GRCh37
NC_000016.8:g.16160974G=	NCBI36
NG_007558.2:g.68856C=
NG_007558.3:g.69002C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3634-33C=	ENSP00000483331.2:n.3634-33C=
ENST00000205557.12:c.3634-33C= MANE Select	ENSP00000205557.7:n.3634-33C=
ENST00000640696.1:c.448-33C=	ENSP00000492197.1:n.448-33C=
ENST00000205557.11:c.3634-33C=	ENSP00000205557.7:n.3634-33C=
ENST00000456970.6:c.3259-33C=	ENSP00000405002.2:n.3259-33C=
ENST00000622290.4:c.*843-33C=	ENSP00000483331.1:n.*843-33C=
NM_001171.5:c.3634-33C=	NP_001162.4:n.3634-33C=
XM_011522479.1:c.3601-33C=	XP_011520781.1:n.3601-33C=
XM_011522480.1:c.3292-33C=	XP_011520782.1:n.3292-33C=
XM_011522481.1:c.3292-33C=	XP_011520783.1:n.3292-33C=
XR_932836.1:n.3869-33C=
XR_932837.1:n.3670-33C=
XR_932838.1:n.3670-33C=
XR_933133.1:n.27G=
XR_933134.1:n.539-165G=
NM_001351800.1:c.3292-33C=	NP_001338729.1:n.3292-33C=
NR_147784.1:n.3296-33C=
XM_011522479.2:c.3601-33C=	XP_011520781.1:n.3601-33C=
XM_011522481.3:c.3292-33C=	XP_011520783.1:n.3292-33C=
XM_017023212.1:c.3466-33C=	XP_016878701.1:n.3466-33C=
XM_024450261.1:c.3670-33C=	XP_024306029.1:n.3670-33C=
XR_932836.2:n.3815-33C=
XR_932837.3:n.3615-33C=
XR_932838.3:n.3615-33C=
NM_001171.6:c.3634-33C= MANE Select	NP_001162.5:n.3634-33C=