Canonical Allele Identifier: CA2210143253

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169707A= , CM000678.2:g.16169707A=	GRCh38
NC_000016.9:g.16263564A= , CM000678.1:g.16263564A=	GRCh37
NC_000016.8:g.16171065A=	NCBI36
NG_007558.2:g.58765T=
NG_007558.3:g.58911T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2934T=	ENSP00000483331.2:p.Gly978=
ENST00000205557.12:c.2934T= MANE Select	ENSP00000205557.7:p.Gly978=
ENST00000205557.11:c.2934T=	ENSP00000205557.7:p.Gly978=
ENST00000456970.6:c.2759T=	ENSP00000405002.2:n.2759T=
ENST00000622290.4:c.*143T=	ENSP00000483331.1:n.*143T=
NM_001171.5:c.2934T=	NP_001162.4:p.Gly978=
XM_011522479.1:c.2901T=	XP_011520781.1:p.Gly967=
XM_011522480.1:c.2592T=	XP_011520782.1:p.Gly864=
XM_011522481.1:c.2592T=	XP_011520783.1:p.Gly864=
XR_932836.1:n.3169T=
XR_932837.1:n.3170T=
XR_932838.1:n.3170T=
NM_001351800.1:c.2592T=	NP_001338729.1:p.Gly864=
NR_147784.1:n.2796T=
XM_011522479.2:c.2901T=	XP_011520781.1:p.Gly967=
XM_011522481.3:c.2592T=	XP_011520783.1:p.Gly864=
XM_017023212.1:c.2766T=	XP_016878701.1:p.Gly922=
XM_017023214.1:c.2934T=	XP_016878703.1:p.Gly978=
XM_024450261.1:c.2970T=	XP_024306029.1:p.Gly990=
XR_932836.2:n.3115T=
XR_932837.3:n.3115T=
XR_932838.3:n.3115T=
NM_001171.6:c.2934T= MANE Select	NP_001162.5:p.Gly978=