Canonical Allele Identifier: CA2210137032

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16163192T= , CM000678.2:g.16163192T=	GRCh38
NC_000016.9:g.16257049T= , CM000678.1:g.16257049T=	GRCh37
NC_000016.8:g.16164550T=	NCBI36
NG_007558.2:g.65280A=
NG_007558.3:g.65426A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3307A=	ENSP00000483331.2:p.Ser1103=
ENST00000205557.12:c.3307A= MANE Select	ENSP00000205557.7:p.Ser1103=
ENST00000640696.1:c.321-1628A=	ENSP00000492197.1:n.321-1628A=
ENST00000205557.11:c.3307A=	ENSP00000205557.7:p.Ser1103=
ENST00000456970.6:c.3132-1628A=	ENSP00000405002.2:n.3132-1628A=
ENST00000622290.4:c.*516A=	ENSP00000483331.1:n.*516A=
NM_001171.5:c.3307A=	NP_001162.4:p.Ser1103=
XM_011522479.1:c.3274A=	XP_011520781.1:p.Ser1092=
XM_011522480.1:c.2965A=	XP_011520782.1:p.Ser989=
XM_011522481.1:c.2965A=	XP_011520783.1:p.Ser989=
XR_932836.1:n.3542A=
XR_932837.1:n.3543-1628A=
XR_932838.1:n.3543-1628A=
XR_933133.1:n.407+349T=
XR_933134.1:n.754+349T=
NM_001351800.1:c.2965A=	NP_001338729.1:p.Ser989=
NR_147784.1:n.3169-1628A=
XM_011522479.2:c.3274A=	XP_011520781.1:p.Ser1092=
XM_011522481.3:c.2965A=	XP_011520783.1:p.Ser989=
XM_017023212.1:c.3139A=	XP_016878701.1:p.Ser1047=
XM_017023214.1:c.3307-1628A=	XP_016878703.1:n.3307-1628A=
XM_024450261.1:c.3343A=	XP_024306029.1:p.Ser1115=
XR_932836.2:n.3488A=
XR_932837.3:n.3488-1628A=
XR_932838.3:n.3488-1628A=
NM_001171.6:c.3307A= MANE Select	NP_001162.5:p.Ser1103=