Canonical Allele Identifier: CA2210143316

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169810G= , CM000678.2:g.16169810G=	GRCh38
NC_000016.9:g.16263667G= , CM000678.1:g.16263667G=	GRCh37
NC_000016.8:g.16171168G=	NCBI36
NG_007558.2:g.58662C=
NG_007558.3:g.58808C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2831C=	ENSP00000483331.2:p.Thr944=
ENST00000205557.12:c.2831C= MANE Select	ENSP00000205557.7:p.Thr944=
ENST00000205557.11:c.2831C=	ENSP00000205557.7:p.Thr944=
ENST00000456970.6:c.2656C=	ENSP00000405002.2:n.2656C=
ENST00000622290.4:c.*40C=	ENSP00000483331.1:n.*40C=
NM_001171.5:c.2831C=	NP_001162.4:p.Thr944=
XM_011522479.1:c.2798C=	XP_011520781.1:p.Thr933=
XM_011522480.1:c.2489C=	XP_011520782.1:p.Thr830=
XM_011522481.1:c.2489C=	XP_011520783.1:p.Thr830=
XR_932836.1:n.3066C=
XR_932837.1:n.3067C=
XR_932838.1:n.3067C=
NM_001351800.1:c.2489C=	NP_001338729.1:p.Thr830=
NR_147784.1:n.2693C=
XM_011522479.2:c.2798C=	XP_011520781.1:p.Thr933=
XM_011522481.3:c.2489C=	XP_011520783.1:p.Thr830=
XM_017023212.1:c.2663C=	XP_016878701.1:p.Thr888=
XM_017023214.1:c.2831C=	XP_016878703.1:p.Thr944=
XM_024450261.1:c.2867C=	XP_024306029.1:p.Thr956=
XR_932836.2:n.3012C=
XR_932837.3:n.3012C=
XR_932838.3:n.3012C=
NM_001171.6:c.2831C= MANE Select	NP_001162.5:p.Thr944=