Canonical Allele Identifier: CA394875847

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16248828G>C (hg19) ; chr16:g.16154971G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154971G>C , CM000678.2:g.16154971G>C	GRCh38
NC_000016.9:g.16248828G>C , CM000678.1:g.16248828G>C	GRCh37
NC_000016.8:g.16156329G>C	NCBI36
NG_007558.2:g.73501C>G
NG_007558.3:g.73647C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.806C>G
ENST00000622290.5:c.*115C>G	ENSP00000483331.2:n.*115C>G
ENST00000205557.12:c.3943C>G MANE Select	ENSP00000205557.7:p.Leu1315Val
ENST00000640696.1:c.757C>G	ENSP00000492197.1:p.Leu253Val
ENST00000205557.11:c.3943C>G	ENSP00000205557.7:p.Leu1315Val
ENST00000456970.6:c.3568C>G	ENSP00000405002.2:n.3568C>G
ENST00000576204.5:n.806C>G
ENST00000622290.4:c.*1152C>G	ENSP00000483331.1:n.*1152C>G
NM_001171.5:c.3943C>G	NP_001162.4:p.Leu1315Val
XM_011522479.1:c.3910C>G	XP_011520781.1:p.Leu1304Val
XM_011522480.1:c.3601C>G	XP_011520782.1:p.Leu1201Val
XM_011522481.1:c.3601C>G	XP_011520783.1:p.Leu1201Val
XR_932836.1:n.4241C>G
XR_932837.1:n.3979C>G
XR_932838.1:n.4042C>G
XR_933134.1:n.539-4810G>C
NM_001351800.1:c.3601C>G	NP_001338729.1:p.Leu1201Val
NR_147784.1:n.3605C>G
XM_011522479.2:c.3910C>G	XP_011520781.1:p.Leu1304Val
XM_011522481.3:c.3601C>G	XP_011520783.1:p.Leu1201Val
XM_017023212.1:c.3775C>G	XP_016878701.1:p.Leu1259Val
XM_024450261.1:c.3979C>G	XP_024306029.1:p.Leu1327Val
XR_932836.2:n.4187C>G
XR_932837.3:n.3924C>G
XR_932838.3:n.3987C>G
NM_001171.6:c.3943C>G MANE Select	NP_001162.5:p.Leu1315Val