Canonical Allele Identifier: CA2210151564

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16192898C= , CM000678.2:g.16192898C=	GRCh38
NC_000016.9:g.16286755C= , CM000678.1:g.16286755C=	GRCh37
NC_000016.8:g.16194256C=	NCBI36
NG_007558.2:g.35574G=
NG_007558.3:g.35720G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001171.6:c.1363G= MANE Select	NP_001162.5:p.Ala455=
ENST00000205557.12:c.1363G= MANE Select	ENSP00000205557.7:p.Ala455=
NM_001171.5:c.1363G=	NP_001162.4:p.Ala455=
NM_001351800.1:c.1021G=	NP_001338729.1:p.Ala341=
NR_147784.1:n.1400G=
ENST00000205557.11:c.1363G=	ENSP00000205557.7:p.Ala455=
ENST00000456970.6:c.1363G=	ENSP00000405002.2:p.Ala455=
ENST00000574094.5:n.1459G=
ENST00000622290.4:c.1363G=	ENSP00000483331.1:p.Ala455=
ENST00000622290.5:c.1363G=	ENSP00000483331.2:p.Ala455=
XM_011522479.1:c.1363G=	XP_011520781.1:p.Ala455=
XM_011522479.2:c.1363G=	XP_011520781.1:p.Ala455=
XM_011522480.1:c.1021G=	XP_011520782.1:p.Ala341=
XM_011522481.1:c.1021G=	XP_011520783.1:p.Ala341=
XM_011522481.3:c.1021G=	XP_011520783.1:p.Ala341=
XM_011522482.1:c.1363G=	XP_011520784.1:p.Ala455=
XM_011522482.3:c.1363G=	XP_011520784.1:p.Ala455=
XM_017023212.1:c.1363G=	XP_016878701.1:p.Ala455=
XM_017023214.1:c.1363G=	XP_016878703.1:p.Ala455=
XM_024450261.1:c.1399G=	XP_024306029.1:p.Ala467=
XR_932836.1:n.1598G=
XR_932836.2:n.1544G=
XR_932837.1:n.1599G=
XR_932837.3:n.1544G=
XR_932838.1:n.1599G=
XR_932838.3:n.1544G=