Canonical Allele Identifier: CA2210141116

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16155041G= , CM000678.2:g.16155041G=	GRCh38
NC_000016.9:g.16248898G= , CM000678.1:g.16248898G=	GRCh37
NC_000016.8:g.16156399G=	NCBI36
NG_007558.2:g.73431C=
NG_007558.3:g.73577C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.736C=
ENST00000622290.5:c.*55-10C=	ENSP00000483331.2:n.*55-10C=
ENST00000205557.12:c.3883-10C= MANE Select	ENSP00000205557.7:n.3883-10C=
ENST00000640696.1:c.697-10C=	ENSP00000492197.1:n.697-10C=
ENST00000205557.11:c.3883-10C=	ENSP00000205557.7:n.3883-10C=
ENST00000456970.6:c.3508-10C=	ENSP00000405002.2:n.3508-10C=
ENST00000576204.5:n.736C=
ENST00000622290.4:c.*1092-10C=	ENSP00000483331.1:n.*1092-10C=
NM_001171.5:c.3883-10C=	NP_001162.4:n.3883-10C=
XM_011522479.1:c.3850-10C=	XP_011520781.1:n.3850-10C=
XM_011522480.1:c.3541-10C=	XP_011520782.1:n.3541-10C=
XM_011522481.1:c.3541-10C=	XP_011520783.1:n.3541-10C=
XR_932836.1:n.4181-10C=
XR_932837.1:n.3919-10C=
XR_932838.1:n.3982-10C=
XR_933134.1:n.539-4740G=
NM_001351800.1:c.3541-10C=	NP_001338729.1:n.3541-10C=
NR_147784.1:n.3545-10C=
XM_011522479.2:c.3850-10C=	XP_011520781.1:n.3850-10C=
XM_011522481.3:c.3541-10C=	XP_011520783.1:n.3541-10C=
XM_017023212.1:c.3715-10C=	XP_016878701.1:n.3715-10C=
XM_024450261.1:c.3919-10C=	XP_024306029.1:n.3919-10C=
XR_932836.2:n.4127-10C=
XR_932837.3:n.3864-10C=
XR_932838.3:n.3927-10C=
NM_001171.6:c.3883-10C= MANE Select	NP_001162.5:n.3883-10C=