Canonical Allele Identifier: CA2210136266

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16162906C= , CM000678.2:g.16162906C=	GRCh38
NC_000016.9:g.16256763C= , CM000678.1:g.16256763C=	GRCh37
NC_000016.8:g.16164264C=	NCBI36
NG_007558.2:g.65566G=
NG_007558.3:g.65712G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3506+87G=	ENSP00000483331.2:n.3506+87G=
ENST00000205557.12:c.3506+87G= MANE Select	ENSP00000205557.7:n.3506+87G=
ENST00000640696.1:c.321-1342G=	ENSP00000492197.1:n.321-1342G=
ENST00000205557.11:c.3506+87G=	ENSP00000205557.7:n.3506+87G=
ENST00000456970.6:c.3132-1342G=	ENSP00000405002.2:n.3132-1342G=
ENST00000622290.4:c.*715+87G=	ENSP00000483331.1:n.*715+87G=
NM_001171.5:c.3506+87G=	NP_001162.4:n.3506+87G=
XM_011522479.1:c.3473+87G=	XP_011520781.1:n.3473+87G=
XM_011522480.1:c.3164+87G=	XP_011520782.1:n.3164+87G=
XM_011522481.1:c.3164+87G=	XP_011520783.1:n.3164+87G=
XR_932836.1:n.3741+87G=
XR_932837.1:n.3543-1342G=
XR_932838.1:n.3543-1342G=
XR_933133.1:n.407+63C=
XR_933134.1:n.754+63C=
NM_001351800.1:c.3164+87G=	NP_001338729.1:n.3164+87G=
NR_147784.1:n.3169-1342G=
XM_011522479.2:c.3473+87G=	XP_011520781.1:n.3473+87G=
XM_011522481.3:c.3164+87G=	XP_011520783.1:n.3164+87G=
XM_017023212.1:c.3338+87G=	XP_016878701.1:n.3338+87G=
XM_017023214.1:c.3307-1342G=	XP_016878703.1:n.3307-1342G=
XM_024450261.1:c.3542+87G=	XP_024306029.1:n.3542+87G=
XR_932836.2:n.3687+87G=
XR_932837.3:n.3488-1342G=
XR_932838.3:n.3488-1342G=
NM_001171.6:c.3506+87G= MANE Select	NP_001162.5:n.3506+87G=