Canonical Allele Identifier: CA2210133337

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16149698T= , CM000678.2:g.16149698T=	GRCh38
NC_000016.9:g.16243555T= , CM000678.1:g.16243555T=	GRCh37
NC_000016.8:g.16151056T=	NCBI36
NG_007558.2:g.78774A=
NG_007558.3:g.78920A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*1119A=	ENSP00000483331.2:n.*1119A=
ENST00000205557.12:c.*435A= MANE Select	ENSP00000205557.7:n.*435A=
ENST00000640696.1:c.1761A=	ENSP00000492197.1:n.1761A=
ENST00000205557.11:c.*435A=	ENSP00000205557.7:n.*435A=
ENST00000576204.5:n.1810A=
ENST00000622290.4:c.*2156A=	ENSP00000483331.1:n.*2156A=
NM_001171.5:c.*435A=	NP_001162.4:n.*435A=
XM_011522479.1:c.*435A=	XP_011520781.1:n.*435A=
XM_011522480.1:c.*435A=	XP_011520782.1:n.*435A=
XM_011522481.1:c.*435A=	XP_011520783.1:n.*435A=
XR_933134.1:n.538+5408T=
NM_001351800.1:c.*435A=	NP_001338729.1:n.*435A=
NR_147784.1:n.4609A=
XM_011522479.2:c.*435A=	XP_011520781.1:n.*435A=
XM_011522481.3:c.*435A=	XP_011520783.1:n.*435A=
XM_017023212.1:c.*435A=	XP_016878701.1:n.*435A=
XM_024450261.1:c.*435A=	XP_024306029.1:n.*435A=
NM_001171.6:c.*435A= MANE Select	NP_001162.5:n.*435A=