Canonical Allele Identifier: CA2210145408

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16173287G= , CM000678.2:g.16173287G=	GRCh38
NC_000016.9:g.16267144G= , CM000678.1:g.16267144G=	GRCh37
NC_000016.8:g.16174645G=	NCBI36
NG_007558.2:g.55185C=
NG_007558.3:g.55331C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2784C=	ENSP00000483331.2:p.Gly928=
ENST00000205557.12:c.2784C= MANE Select	ENSP00000205557.7:p.Gly928=
ENST00000205557.11:c.2784C=	ENSP00000205557.7:p.Gly928=
ENST00000456970.6:c.2609C=	ENSP00000405002.2:p.Ala870=
ENST00000576683.1:n.271C=
ENST00000622290.4:c.2609C=	ENSP00000483331.1:p.Ala870=
NM_001171.5:c.2784C=	NP_001162.4:p.Gly928=
XM_011522479.1:c.2751C=	XP_011520781.1:p.Gly917=
XM_011522480.1:c.2442C=	XP_011520782.1:p.Gly814=
XM_011522481.1:c.2442C=	XP_011520783.1:p.Gly814=
XR_932836.1:n.3019C=
XR_932837.1:n.3020C=
XR_932838.1:n.3020C=
NM_001351800.1:c.2442C=	NP_001338729.1:p.Gly814=
NR_147784.1:n.2646C=
XM_011522479.2:c.2751C=	XP_011520781.1:p.Gly917=
XM_011522481.3:c.2442C=	XP_011520783.1:p.Gly814=
XM_017023212.1:c.2616C=	XP_016878701.1:p.Gly872=
XM_017023214.1:c.2784C=	XP_016878703.1:p.Gly928=
XM_024450261.1:c.2820C=	XP_024306029.1:p.Gly940=
XR_932836.2:n.2965C=
XR_932837.3:n.2965C=
XR_932838.3:n.2965C=
NM_001171.6:c.2784C= MANE Select	NP_001162.5:p.Gly928=