Canonical Allele Identifier: CA2210141075

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16155022C= , CM000678.2:g.16155022C=	GRCh38
NC_000016.9:g.16248879C= , CM000678.1:g.16248879C=	GRCh37
NC_000016.8:g.16156380C=	NCBI36
NG_007558.2:g.73450G=
NG_007558.3:g.73596G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000576204.6:n.755G=
ENST00000622290.5:c.*64G=	ENSP00000483331.2:n.*64G=
ENST00000205557.12:c.3892G= MANE Select	ENSP00000205557.7:p.Val1298=
ENST00000640696.1:c.706G=	ENSP00000492197.1:p.Val236=
ENST00000205557.11:c.3892G=	ENSP00000205557.7:p.Val1298=
ENST00000456970.6:c.3517G=	ENSP00000405002.2:n.3517G=
ENST00000576204.5:n.755G=
ENST00000622290.4:c.*1101G=	ENSP00000483331.1:n.*1101G=
NM_001171.5:c.3892G=	NP_001162.4:p.Val1298=
XM_011522479.1:c.3859G=	XP_011520781.1:p.Val1287=
XM_011522480.1:c.3550G=	XP_011520782.1:p.Val1184=
XM_011522481.1:c.3550G=	XP_011520783.1:p.Val1184=
XR_932836.1:n.4190G=
XR_932837.1:n.3928G=
XR_932838.1:n.3991G=
XR_933134.1:n.539-4759C=
NM_001351800.1:c.3550G=	NP_001338729.1:p.Val1184=
NR_147784.1:n.3554G=
XM_011522479.2:c.3859G=	XP_011520781.1:p.Val1287=
XM_011522481.3:c.3550G=	XP_011520783.1:p.Val1184=
XM_017023212.1:c.3724G=	XP_016878701.1:p.Val1242=
XM_024450261.1:c.3928G=	XP_024306029.1:p.Val1310=
XR_932836.2:n.4136G=
XR_932837.3:n.3873G=
XR_932838.3:n.3936G=
NM_001171.6:c.3892G= MANE Select	NP_001162.5:p.Val1298=