Canonical Allele Identifier: CA2210134618

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150518C= , CM000678.2:g.16150518C=	GRCh38
NC_000016.9:g.16244375C= , CM000678.1:g.16244375C=	GRCh37
NC_000016.8:g.16151876C=	NCBI36
NG_007558.2:g.77954G=
NG_007558.3:g.78100G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*575+60G=	ENSP00000483331.2:n.*575+60G=
ENST00000205557.12:c.4403+60G= MANE Select	ENSP00000205557.7:n.4403+60G=
ENST00000640696.1:c.1217+60G=	ENSP00000492197.1:n.1217+60G=
ENST00000205557.11:c.4403+60G=	ENSP00000205557.7:n.4403+60G=
ENST00000456970.6:c.4028+60G=	ENSP00000405002.2:n.4028+60G=
ENST00000576204.5:n.1266+60G=
ENST00000622290.4:c.*1612+60G=	ENSP00000483331.1:n.*1612+60G=
NM_001171.5:c.4403+60G=	NP_001162.4:n.4403+60G=
XM_011522479.1:c.4370+60G=	XP_011520781.1:n.4370+60G=
XM_011522480.1:c.4061+60G=	XP_011520782.1:n.4061+60G=
XM_011522481.1:c.4061+60G=	XP_011520783.1:n.4061+60G=
XR_933134.1:n.538+6228C=
NM_001351800.1:c.4061+60G=	NP_001338729.1:n.4061+60G=
NR_147784.1:n.4065+60G=
XM_011522479.2:c.4370+60G=	XP_011520781.1:n.4370+60G=
XM_011522481.3:c.4061+60G=	XP_011520783.1:n.4061+60G=
XM_017023212.1:c.4235+60G=	XP_016878701.1:n.4235+60G=
XM_024450261.1:c.4439+60G=	XP_024306029.1:n.4439+60G=
NM_001171.6:c.4403+60G= MANE Select	NP_001162.5:n.4403+60G=