Canonical Allele Identifier: CA2210141389

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16155331C= , CM000678.2:g.16155331C=	GRCh38
NC_000016.9:g.16249188C= , CM000678.1:g.16249188C=	GRCh37
NC_000016.8:g.16156689C=	NCBI36
NG_007558.2:g.73141G=
NG_007558.3:g.73287G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.446G=
ENST00000622290.5:c.*55-300G=	ENSP00000483331.2:n.*55-300G=
ENST00000205557.12:c.3883-300G= MANE Select	ENSP00000205557.7:n.3883-300G=
ENST00000640696.1:c.697-300G=	ENSP00000492197.1:n.697-300G=
ENST00000205557.11:c.3883-300G=	ENSP00000205557.7:n.3883-300G=
ENST00000456970.6:c.3508-300G=	ENSP00000405002.2:n.3508-300G=
ENST00000576204.5:n.446G=
ENST00000622290.4:c.*1092-300G=	ENSP00000483331.1:n.*1092-300G=
NM_001171.5:c.3883-300G=	NP_001162.4:n.3883-300G=
XM_011522479.1:c.3850-300G=	XP_011520781.1:n.3850-300G=
XM_011522480.1:c.3541-300G=	XP_011520782.1:n.3541-300G=
XM_011522481.1:c.3541-300G=	XP_011520783.1:n.3541-300G=
XR_932836.1:n.4181-300G=
XR_932837.1:n.3919-300G=
XR_932838.1:n.3982-300G=
XR_933134.1:n.539-4450C=
NM_001351800.1:c.3541-300G=	NP_001338729.1:n.3541-300G=
NR_147784.1:n.3545-300G=
XM_011522479.2:c.3850-300G=	XP_011520781.1:n.3850-300G=
XM_011522481.3:c.3541-300G=	XP_011520783.1:n.3541-300G=
XM_017023212.1:c.3715-300G=	XP_016878701.1:n.3715-300G=
XM_024450261.1:c.3919-300G=	XP_024306029.1:n.3919-300G=
XR_932836.2:n.4127-300G=
XR_932837.3:n.3864-300G=
XR_932838.3:n.3927-300G=
NM_001171.6:c.3883-300G= MANE Select	NP_001162.5:n.3883-300G=