Canonical Allele Identifier: CA2210134576

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16161463C= , CM000678.2:g.16161463C=	GRCh38
NC_000016.9:g.16255320C= , CM000678.1:g.16255320C=	GRCh37
NC_000016.8:g.16162821C=	NCBI36
NG_007558.2:g.67009G=
NG_007558.3:g.67155G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001171.6:c.3608G= MANE Select	NP_001162.5:p.Gly1203=
ENST00000205557.12:c.3608G= MANE Select	ENSP00000205557.7:p.Gly1203=
NM_001171.5:c.3608G=	NP_001162.4:p.Gly1203=
NM_001351800.1:c.3266G=	NP_001338729.1:p.Gly1089=
NR_147784.1:n.3270G=
ENST00000205557.11:c.3608G=	ENSP00000205557.7:p.Gly1203=
ENST00000456970.6:c.3233G=	ENSP00000405002.2:n.3233G=
ENST00000622290.4:c.*817G=	ENSP00000483331.1:n.*817G=
ENST00000622290.5:c.3608G=	ENSP00000483331.2:p.Gly1203=
ENST00000640696.1:c.422G=	ENSP00000492197.1:p.Gly141=
XM_011522479.1:c.3575G=	XP_011520781.1:p.Gly1192=
XM_011522479.2:c.3575G=	XP_011520781.1:p.Gly1192=
XM_011522480.1:c.3266G=	XP_011520782.1:p.Gly1089=
XM_011522481.1:c.3266G=	XP_011520783.1:p.Gly1089=
XM_011522481.3:c.3266G=	XP_011520783.1:p.Gly1089=
XM_017023212.1:c.3440G=	XP_016878701.1:p.Gly1147=
XM_017023214.1:c.3408G=	XP_016878703.1:p.Gly1136=
XM_024450261.1:c.3644G=	XP_024306029.1:p.Gly1215=
XR_932836.1:n.3843G=
XR_932836.2:n.3789G=
XR_932837.1:n.3644G=
XR_932837.3:n.3589G=
XR_932838.1:n.3644G=
XR_932838.3:n.3589G=
XR_933133.1:n.260-1233C=
XR_933134.1:n.607-1233C=