Canonical Allele Identifier: CA2210140883

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154904G= , CM000678.2:g.16154904G=	GRCh38
NC_000016.9:g.16248761G= , CM000678.1:g.16248761G=	GRCh37
NC_000016.8:g.16156262G=	NCBI36
NG_007558.2:g.73568C=
NG_007558.3:g.73714C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.873C=
ENST00000622290.5:c.*182C=	ENSP00000483331.2:n.*182C=
ENST00000205557.12:c.4010C= MANE Select	ENSP00000205557.7:p.Thr1337=
ENST00000640696.1:c.824C=	ENSP00000492197.1:p.Thr275=
ENST00000205557.11:c.4010C=	ENSP00000205557.7:p.Thr1337=
ENST00000456970.6:c.3635C=	ENSP00000405002.2:n.3635C=
ENST00000576204.5:n.873C=
ENST00000622290.4:c.*1219C=	ENSP00000483331.1:n.*1219C=
NM_001171.5:c.4010C=	NP_001162.4:p.Thr1337=
XM_011522479.1:c.3977C=	XP_011520781.1:p.Thr1326=
XM_011522480.1:c.3668C=	XP_011520782.1:p.Thr1223=
XM_011522481.1:c.3668C=	XP_011520783.1:p.Thr1223=
XR_933134.1:n.539-4877G=
NM_001351800.1:c.3668C=	NP_001338729.1:p.Thr1223=
NR_147784.1:n.3672C=
XM_011522479.2:c.3977C=	XP_011520781.1:p.Thr1326=
XM_011522481.3:c.3668C=	XP_011520783.1:p.Thr1223=
XM_017023212.1:c.3842C=	XP_016878701.1:p.Thr1281=
XM_024450261.1:c.4046C=	XP_024306029.1:p.Thr1349=
NM_001171.6:c.4010C= MANE Select	NP_001162.5:p.Thr1337=