Canonical Allele Identifier: CA2210139887

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16165699C= , CM000678.2:g.16165699C=	GRCh38
NC_000016.9:g.16259556C= , CM000678.1:g.16259556C=	GRCh37
NC_000016.8:g.16167057C=	NCBI36
NG_007558.2:g.62773G=
NG_007558.3:g.62919G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3230G=	ENSP00000483331.2:p.Ser1077=
ENST00000205557.12:c.3230G= MANE Select	ENSP00000205557.7:p.Ser1077=
ENST00000640696.1:c.245G=	ENSP00000492197.1:p.Ser82=
ENST00000205557.11:c.3230G=	ENSP00000205557.7:p.Ser1077=
ENST00000456970.6:c.3055G=	ENSP00000405002.2:n.3055G=
ENST00000622290.4:c.*439G=	ENSP00000483331.1:n.*439G=
NM_001171.5:c.3230G=	NP_001162.4:p.Ser1077=
XM_011522479.1:c.3197G=	XP_011520781.1:p.Ser1066=
XM_011522480.1:c.2888G=	XP_011520782.1:p.Ser963=
XM_011522481.1:c.2888G=	XP_011520783.1:p.Ser963=
XR_932836.1:n.3465G=
XR_932837.1:n.3466G=
XR_932838.1:n.3466G=
NM_001351800.1:c.2888G=	NP_001338729.1:p.Ser963=
NR_147784.1:n.3092G=
XM_011522479.2:c.3197G=	XP_011520781.1:p.Ser1066=
XM_011522481.3:c.2888G=	XP_011520783.1:p.Ser963=
XM_017023212.1:c.3062G=	XP_016878701.1:p.Ser1021=
XM_017023214.1:c.3230G=	XP_016878703.1:p.Ser1077=
XM_024450261.1:c.3266G=	XP_024306029.1:p.Ser1089=
XR_932836.2:n.3411G=
XR_932837.3:n.3411G=
XR_932838.3:n.3411G=
NM_001171.6:c.3230G= MANE Select	NP_001162.5:p.Ser1077=