Canonical Allele Identifier: CA2210155049

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16202033G= , CM000678.2:g.16202033G=	GRCh38
NC_000016.9:g.16295890G= , CM000678.1:g.16295890G=	GRCh37
NC_000016.8:g.16203391G=	NCBI36
NG_007558.2:g.26439C=
NG_007558.3:g.26585C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001171.6:c.1144C= MANE Select	NP_001162.5:p.Arg382=
ENST00000205557.12:c.1144C= MANE Select	ENSP00000205557.7:p.Arg382=
NM_001171.5:c.1144C=	NP_001162.4:p.Arg382=
NM_001351800.1:c.802C=	NP_001338729.1:p.Arg268=
NR_147784.1:n.1181C=
ENST00000205557.11:c.1144C=	ENSP00000205557.7:p.Arg382=
ENST00000456970.6:c.1144C=	ENSP00000405002.2:p.Arg382=
ENST00000574094.5:n.1240C=
ENST00000574094.6:c.1144C=	ENSP00000507301.1:p.Arg382=
ENST00000577103.1:c.*1011C=	ENSP00000459243.1:n.*1011C=
ENST00000622290.4:c.1144C=	ENSP00000483331.1:p.Arg382=
ENST00000622290.5:c.1144C=	ENSP00000483331.2:p.Arg382=
XM_011522479.1:c.1144C=	XP_011520781.1:p.Arg382=
XM_011522479.2:c.1144C=	XP_011520781.1:p.Arg382=
XM_011522480.1:c.802C=	XP_011520782.1:p.Arg268=
XM_011522481.1:c.802C=	XP_011520783.1:p.Arg268=
XM_011522481.3:c.802C=	XP_011520783.1:p.Arg268=
XM_011522482.1:c.1144C=	XP_011520784.1:p.Arg382=
XM_011522482.3:c.1144C=	XP_011520784.1:p.Arg382=
XM_017023212.1:c.1144C=	XP_016878701.1:p.Arg382=
XM_017023214.1:c.1144C=	XP_016878703.1:p.Arg382=
XM_024450261.1:c.1180C=	XP_024306029.1:p.Arg394=
XR_932836.1:n.1379C=
XR_932836.2:n.1325C=
XR_932837.1:n.1380C=
XR_932837.3:n.1325C=
XR_932838.1:n.1380C=
XR_932838.3:n.1325C=