Canonical Allele Identifier: CA2210136739

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16163099T= , CM000678.2:g.16163099T=	GRCh38
NC_000016.9:g.16256956T= , CM000678.1:g.16256956T=	GRCh37
NC_000016.8:g.16164457T=	NCBI36
NG_007558.2:g.65373A=
NG_007558.3:g.65519A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3400A=	ENSP00000483331.2:p.Ser1134=
ENST00000205557.12:c.3400A= MANE Select	ENSP00000205557.7:p.Ser1134=
ENST00000640696.1:c.321-1535A=	ENSP00000492197.1:n.321-1535A=
ENST00000205557.11:c.3400A=	ENSP00000205557.7:p.Ser1134=
ENST00000456970.6:c.3132-1535A=	ENSP00000405002.2:n.3132-1535A=
ENST00000622290.4:c.*609A=	ENSP00000483331.1:n.*609A=
NM_001171.5:c.3400A=	NP_001162.4:p.Ser1134=
XM_011522479.1:c.3367A=	XP_011520781.1:p.Ser1123=
XM_011522480.1:c.3058A=	XP_011520782.1:p.Ser1020=
XM_011522481.1:c.3058A=	XP_011520783.1:p.Ser1020=
XR_932836.1:n.3635A=
XR_932837.1:n.3543-1535A=
XR_932838.1:n.3543-1535A=
XR_933133.1:n.407+256T=
XR_933134.1:n.754+256T=
NM_001351800.1:c.3058A=	NP_001338729.1:p.Ser1020=
NR_147784.1:n.3169-1535A=
XM_011522479.2:c.3367A=	XP_011520781.1:p.Ser1123=
XM_011522481.3:c.3058A=	XP_011520783.1:p.Ser1020=
XM_017023212.1:c.3232A=	XP_016878701.1:p.Ser1078=
XM_017023214.1:c.3307-1535A=	XP_016878703.1:n.3307-1535A=
XM_024450261.1:c.3436A=	XP_024306029.1:p.Ser1146=
XR_932836.2:n.3581A=
XR_932837.3:n.3488-1535A=
XR_932838.3:n.3488-1535A=
NM_001171.6:c.3400A= MANE Select	NP_001162.5:p.Ser1134=