Canonical Allele Identifier: CA2210140830

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154881T= , CM000678.2:g.16154881T=	GRCh38
NC_000016.9:g.16248738T= , CM000678.1:g.16248738T=	GRCh37
NC_000016.8:g.16156239T=	NCBI36
NG_007558.2:g.73591A=
NG_007558.3:g.73737A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.896A=
ENST00000622290.5:c.*205A=	ENSP00000483331.2:n.*205A=
ENST00000205557.12:c.4033A= MANE Select	ENSP00000205557.7:p.Ile1345=
ENST00000640696.1:c.847A=	ENSP00000492197.1:p.Ile283=
ENST00000205557.11:c.4033A=	ENSP00000205557.7:p.Ile1345=
ENST00000456970.6:c.3658A=	ENSP00000405002.2:n.3658A=
ENST00000576204.5:n.896A=
ENST00000622290.4:c.*1242A=	ENSP00000483331.1:n.*1242A=
NM_001171.5:c.4033A=	NP_001162.4:p.Ile1345=
XM_011522479.1:c.4000A=	XP_011520781.1:p.Ile1334=
XM_011522480.1:c.3691A=	XP_011520782.1:p.Ile1231=
XM_011522481.1:c.3691A=	XP_011520783.1:p.Ile1231=
XR_933134.1:n.539-4900T=
NM_001351800.1:c.3691A=	NP_001338729.1:p.Ile1231=
NR_147784.1:n.3695A=
XM_011522479.2:c.4000A=	XP_011520781.1:p.Ile1334=
XM_011522481.3:c.3691A=	XP_011520783.1:p.Ile1231=
XM_017023212.1:c.3865A=	XP_016878701.1:p.Ile1289=
XM_024450261.1:c.4069A=	XP_024306029.1:p.Ile1357=
NM_001171.6:c.4033A= MANE Select	NP_001162.5:p.Ile1345=