Canonical Allele Identifier: CA2210143318

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169815C= , CM000678.2:g.16169815C=	GRCh38
NC_000016.9:g.16263672C= , CM000678.1:g.16263672C=	GRCh37
NC_000016.8:g.16171173C=	NCBI36
NG_007558.2:g.58657G=
NG_007558.3:g.58803G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2826G=	ENSP00000483331.2:p.Val942=
ENST00000205557.12:c.2826G= MANE Select	ENSP00000205557.7:p.Val942=
ENST00000205557.11:c.2826G=	ENSP00000205557.7:p.Val942=
ENST00000456970.6:c.2651G=	ENSP00000405002.2:n.2651G=
ENST00000622290.4:c.*35G=	ENSP00000483331.1:n.*35G=
NM_001171.5:c.2826G=	NP_001162.4:p.Val942=
XM_011522479.1:c.2793G=	XP_011520781.1:p.Val931=
XM_011522480.1:c.2484G=	XP_011520782.1:p.Val828=
XM_011522481.1:c.2484G=	XP_011520783.1:p.Val828=
XR_932836.1:n.3061G=
XR_932837.1:n.3062G=
XR_932838.1:n.3062G=
NM_001351800.1:c.2484G=	NP_001338729.1:p.Val828=
NR_147784.1:n.2688G=
XM_011522479.2:c.2793G=	XP_011520781.1:p.Val931=
XM_011522481.3:c.2484G=	XP_011520783.1:p.Val828=
XM_017023212.1:c.2658G=	XP_016878701.1:p.Val886=
XM_017023214.1:c.2826G=	XP_016878703.1:p.Val942=
XM_024450261.1:c.2862G=	XP_024306029.1:p.Val954=
XR_932836.2:n.3007G=
XR_932837.3:n.3007G=
XR_932838.3:n.3007G=
NM_001171.6:c.2826G= MANE Select	NP_001162.5:p.Val942=