Canonical Allele Identifier: CA2210149756

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16182878C= , CM000678.2:g.16182878C=	GRCh38
NC_000016.9:g.16276735C= , CM000678.1:g.16276735C=	GRCh37
NC_000016.8:g.16184236C=	NCBI36
NG_007558.2:g.45594G=
NG_007558.3:g.45740G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001171.6:c.1996G= MANE Select	NP_001162.5:p.Gly666=
ENST00000205557.12:c.1996G= MANE Select	ENSP00000205557.7:p.Gly666=
NM_001171.5:c.1996G=	NP_001162.4:p.Gly666=
NM_001351800.1:c.1654G=	NP_001338729.1:p.Gly552=
NR_147784.1:n.2033G=
ENST00000205557.11:c.1996G=	ENSP00000205557.7:p.Gly666=
ENST00000456970.6:c.1996G=	ENSP00000405002.2:p.Gly666=
ENST00000574094.5:n.2040-953G=
ENST00000622290.4:c.1996G=	ENSP00000483331.1:p.Gly666=
ENST00000622290.5:c.1996G=	ENSP00000483331.2:p.Gly666=
XM_011522479.1:c.1996G=	XP_011520781.1:p.Gly666=
XM_011522479.2:c.1996G=	XP_011520781.1:p.Gly666=
XM_011522480.1:c.1654G=	XP_011520782.1:p.Gly552=
XM_011522481.1:c.1654G=	XP_011520783.1:p.Gly552=
XM_011522481.3:c.1654G=	XP_011520783.1:p.Gly552=
XM_011522482.1:c.1996G=	XP_011520784.1:p.Gly666=
XM_011522482.3:c.1996G=	XP_011520784.1:p.Gly666=
XM_017023212.1:c.1996G=	XP_016878701.1:p.Gly666=
XM_017023214.1:c.1996G=	XP_016878703.1:p.Gly666=
XM_024450261.1:c.2032G=	XP_024306029.1:p.Gly678=
XR_932836.1:n.2231G=
XR_932836.2:n.2177G=
XR_932837.1:n.2232G=
XR_932837.3:n.2177G=
XR_932838.1:n.2232G=
XR_932838.3:n.2177G=