Canonical Allele Identifier: CA2210133353

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16149717A= , CM000678.2:g.16149717A=	GRCh38
NC_000016.9:g.16243574A= , CM000678.1:g.16243574A=	GRCh37
NC_000016.8:g.16151075A=	NCBI36
NG_007558.2:g.78755T=
NG_007558.3:g.78901T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*1100T=	ENSP00000483331.2:n.*1100T=
ENST00000205557.12:c.*416T= MANE Select	ENSP00000205557.7:n.*416T=
ENST00000640696.1:c.1742T=	ENSP00000492197.1:n.1742T=
ENST00000205557.11:c.*416T=	ENSP00000205557.7:n.*416T=
ENST00000576204.5:n.1791T=
ENST00000622290.4:c.*2137T=	ENSP00000483331.1:n.*2137T=
NM_001171.5:c.*416T=	NP_001162.4:n.*416T=
XM_011522479.1:c.*416T=	XP_011520781.1:n.*416T=
XM_011522480.1:c.*416T=	XP_011520782.1:n.*416T=
XM_011522481.1:c.*416T=	XP_011520783.1:n.*416T=
XR_933134.1:n.538+5427A=
NM_001351800.1:c.*416T=	NP_001338729.1:n.*416T=
NR_147784.1:n.4590T=
XM_011522479.2:c.*416T=	XP_011520781.1:n.*416T=
XM_011522481.3:c.*416T=	XP_011520783.1:n.*416T=
XM_017023212.1:c.*416T=	XP_016878701.1:n.*416T=
XM_024450261.1:c.*416T=	XP_024306029.1:n.*416T=
NM_001171.6:c.*416T= MANE Select	NP_001162.5:n.*416T=