Canonical Allele Identifier: CA2210140599

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154765C= , CM000678.2:g.16154765C=	GRCh38
NC_000016.9:g.16248622C= , CM000678.1:g.16248622C=	GRCh37
NC_000016.8:g.16156123C=	NCBI36
NG_007558.2:g.73707G=
NG_007558.3:g.73853G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.934G=
ENST00000622290.5:c.*243G=	ENSP00000483331.2:n.*243G=
ENST00000205557.12:c.4071G= MANE Select	ENSP00000205557.7:p.Arg1357=
ENST00000640696.1:c.885G=	ENSP00000492197.1:p.Arg295=
ENST00000205557.11:c.4071G=	ENSP00000205557.7:p.Arg1357=
ENST00000456970.6:c.3696G=	ENSP00000405002.2:n.3696G=
ENST00000576204.5:n.934G=
ENST00000622290.4:c.*1280G=	ENSP00000483331.1:n.*1280G=
NM_001171.5:c.4071G=	NP_001162.4:p.Arg1357=
XM_011522479.1:c.4038G=	XP_011520781.1:p.Arg1346=
XM_011522480.1:c.3729G=	XP_011520782.1:p.Arg1243=
XM_011522481.1:c.3729G=	XP_011520783.1:p.Arg1243=
XR_933134.1:n.539-5016C=
NM_001351800.1:c.3729G=	NP_001338729.1:p.Arg1243=
NR_147784.1:n.3733G=
XM_011522479.2:c.4038G=	XP_011520781.1:p.Arg1346=
XM_011522481.3:c.3729G=	XP_011520783.1:p.Arg1243=
XM_017023212.1:c.3903G=	XP_016878701.1:p.Arg1301=
XM_024450261.1:c.4107G=	XP_024306029.1:p.Arg1369=
NM_001171.6:c.4071G= MANE Select	NP_001162.5:p.Arg1357=