Canonical Allele Identifier: CA2210134828

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16161567G= , CM000678.2:g.16161567G=	GRCh38
NC_000016.9:g.16255424G= , CM000678.1:g.16255424G=	GRCh37
NC_000016.8:g.16162925G=	NCBI36
NG_007558.2:g.66905C=
NG_007558.3:g.67051C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001171.6:c.3507-3C= MANE Select	NP_001162.5:n.3507-3C=
ENST00000205557.12:c.3507-3C= MANE Select	ENSP00000205557.7:n.3507-3C=
NM_001171.5:c.3507-3C=	NP_001162.4:n.3507-3C=
NM_001351800.1:c.3165-3C=	NP_001338729.1:n.3165-3C=
NR_147784.1:n.3169-3C=
ENST00000205557.11:c.3507-3C=	ENSP00000205557.7:n.3507-3C=
ENST00000456970.6:c.3132-3C=	ENSP00000405002.2:n.3132-3C=
ENST00000622290.4:c.*716-3C=	ENSP00000483331.1:n.*716-3C=
ENST00000622290.5:c.3507-3C=	ENSP00000483331.2:n.3507-3C=
ENST00000640696.1:c.321-3C=	ENSP00000492197.1:n.321-3C=
XM_011522479.1:c.3474-3C=	XP_011520781.1:n.3474-3C=
XM_011522479.2:c.3474-3C=	XP_011520781.1:n.3474-3C=
XM_011522480.1:c.3165-3C=	XP_011520782.1:n.3165-3C=
XM_011522481.1:c.3165-3C=	XP_011520783.1:n.3165-3C=
XM_011522481.3:c.3165-3C=	XP_011520783.1:n.3165-3C=
XM_017023212.1:c.3339-3C=	XP_016878701.1:n.3339-3C=
XM_017023214.1:c.3307-3C=	XP_016878703.1:n.3307-3C=
XM_024450261.1:c.3543-3C=	XP_024306029.1:n.3543-3C=
XR_932836.1:n.3742-3C=
XR_932836.2:n.3688-3C=
XR_932837.1:n.3543-3C=
XR_932837.3:n.3488-3C=
XR_932838.1:n.3543-3C=
XR_932838.3:n.3488-3C=
XR_933133.1:n.260-1129G=
XR_933134.1:n.607-1129G=