Canonical Allele Identifier: CA2210143272

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169734G= , CM000678.2:g.16169734G=	GRCh38
NC_000016.9:g.16263591G= , CM000678.1:g.16263591G=	GRCh37
NC_000016.8:g.16171092G=	NCBI36
NG_007558.2:g.58738C=
NG_007558.3:g.58884C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2907C=	ENSP00000483331.2:p.Ser969=
ENST00000205557.12:c.2907C= MANE Select	ENSP00000205557.7:p.Ser969=
ENST00000205557.11:c.2907C=	ENSP00000205557.7:p.Ser969=
ENST00000456970.6:c.2732C=	ENSP00000405002.2:n.2732C=
ENST00000622290.4:c.*116C=	ENSP00000483331.1:n.*116C=
NM_001171.5:c.2907C=	NP_001162.4:p.Ser969=
XM_011522479.1:c.2874C=	XP_011520781.1:p.Ser958=
XM_011522480.1:c.2565C=	XP_011520782.1:p.Ser855=
XM_011522481.1:c.2565C=	XP_011520783.1:p.Ser855=
XR_932836.1:n.3142C=
XR_932837.1:n.3143C=
XR_932838.1:n.3143C=
NM_001351800.1:c.2565C=	NP_001338729.1:p.Ser855=
NR_147784.1:n.2769C=
XM_011522479.2:c.2874C=	XP_011520781.1:p.Ser958=
XM_011522481.3:c.2565C=	XP_011520783.1:p.Ser855=
XM_017023212.1:c.2739C=	XP_016878701.1:p.Ser913=
XM_017023214.1:c.2907C=	XP_016878703.1:p.Ser969=
XM_024450261.1:c.2943C=	XP_024306029.1:p.Ser981=
XR_932836.2:n.3088C=
XR_932837.3:n.3088C=
XR_932838.3:n.3088C=
NM_001171.6:c.2907C= MANE Select	NP_001162.5:p.Ser969=