Canonical Allele Identifier: CA2210143262

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169720T= , CM000678.2:g.16169720T=	GRCh38
NC_000016.9:g.16263577T= , CM000678.1:g.16263577T=	GRCh37
NC_000016.8:g.16171078T=	NCBI36
NG_007558.2:g.58752A=
NG_007558.3:g.58898A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2921A=	ENSP00000483331.2:p.Asp974=
ENST00000205557.12:c.2921A= MANE Select	ENSP00000205557.7:p.Asp974=
ENST00000205557.11:c.2921A=	ENSP00000205557.7:p.Asp974=
ENST00000456970.6:c.2746A=	ENSP00000405002.2:n.2746A=
ENST00000622290.4:c.*130A=	ENSP00000483331.1:n.*130A=
NM_001171.5:c.2921A=	NP_001162.4:p.Asp974=
XM_011522479.1:c.2888A=	XP_011520781.1:p.Asp963=
XM_011522480.1:c.2579A=	XP_011520782.1:p.Asp860=
XM_011522481.1:c.2579A=	XP_011520783.1:p.Asp860=
XR_932836.1:n.3156A=
XR_932837.1:n.3157A=
XR_932838.1:n.3157A=
NM_001351800.1:c.2579A=	NP_001338729.1:p.Asp860=
NR_147784.1:n.2783A=
XM_011522479.2:c.2888A=	XP_011520781.1:p.Asp963=
XM_011522481.3:c.2579A=	XP_011520783.1:p.Asp860=
XM_017023212.1:c.2753A=	XP_016878701.1:p.Asp918=
XM_017023214.1:c.2921A=	XP_016878703.1:p.Asp974=
XM_024450261.1:c.2957A=	XP_024306029.1:p.Asp986=
XR_932836.2:n.3102A=
XR_932837.3:n.3102A=
XR_932838.3:n.3102A=
NM_001171.6:c.2921A= MANE Select	NP_001162.5:p.Asp974=