Canonical Allele Identifier: CA2210135380

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150768C= , CM000678.2:g.16150768C=	GRCh38
NC_000016.9:g.16244625C= , CM000678.1:g.16244625C=	GRCh37
NC_000016.8:g.16152126C=	NCBI36
NG_007558.2:g.77704G=
NG_007558.3:g.77850G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*385G=	ENSP00000483331.2:n.*385G=
ENST00000205557.12:c.4213G= MANE Select	ENSP00000205557.7:p.Gly1405=
ENST00000640696.1:c.1027G=	ENSP00000492197.1:p.Gly343=
ENST00000205557.11:c.4213G=	ENSP00000205557.7:p.Gly1405=
ENST00000456970.6:c.3838G=	ENSP00000405002.2:n.3838G=
ENST00000576204.5:n.1076G=
ENST00000622290.4:c.*1422G=	ENSP00000483331.1:n.*1422G=
NM_001171.5:c.4213G=	NP_001162.4:p.Gly1405=
XM_011522479.1:c.4180G=	XP_011520781.1:p.Gly1394=
XM_011522480.1:c.3871G=	XP_011520782.1:p.Gly1291=
XM_011522481.1:c.3871G=	XP_011520783.1:p.Gly1291=
XR_933134.1:n.538+6478C=
NM_001351800.1:c.3871G=	NP_001338729.1:p.Gly1291=
NR_147784.1:n.3875G=
XM_011522479.2:c.4180G=	XP_011520781.1:p.Gly1394=
XM_011522481.3:c.3871G=	XP_011520783.1:p.Gly1291=
XM_017023212.1:c.4045G=	XP_016878701.1:p.Gly1349=
XM_024450261.1:c.4249G=	XP_024306029.1:p.Gly1417=
NM_001171.6:c.4213G= MANE Select	NP_001162.5:p.Gly1405=