Canonical Allele Identifier: CA394883888

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16244540T>A (hg19) ; chr16:g.16150683T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150683T>A , CM000678.2:g.16150683T>A	GRCh38
NC_000016.9:g.16244540T>A , CM000678.1:g.16244540T>A	GRCh37
NC_000016.8:g.16152041T>A	NCBI36
NG_007558.2:g.77789A>T
NG_007558.3:g.77935A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*470A>T	ENSP00000483331.2:n.*470A>T
ENST00000205557.12:c.4298A>T MANE Select	ENSP00000205557.7:p.Asp1433Val
ENST00000640696.1:c.1112A>T	ENSP00000492197.1:p.Asp371Val
ENST00000205557.11:c.4298A>T	ENSP00000205557.7:p.Asp1433Val
ENST00000456970.6:c.3923A>T	ENSP00000405002.2:n.3923A>T
ENST00000576204.5:n.1161A>T
ENST00000622290.4:c.*1507A>T	ENSP00000483331.1:n.*1507A>T
NM_001171.5:c.4298A>T	NP_001162.4:p.Asp1433Val
XM_011522479.1:c.4265A>T	XP_011520781.1:p.Asp1422Val
XM_011522480.1:c.3956A>T	XP_011520782.1:p.Asp1319Val
XM_011522481.1:c.3956A>T	XP_011520783.1:p.Asp1319Val
XR_933134.1:n.538+6393T>A
NM_001351800.1:c.3956A>T	NP_001338729.1:p.Asp1319Val
NR_147784.1:n.3960A>T
XM_011522479.2:c.4265A>T	XP_011520781.1:p.Asp1422Val
XM_011522481.3:c.3956A>T	XP_011520783.1:p.Asp1319Val
XM_017023212.1:c.4130A>T	XP_016878701.1:p.Asp1377Val
XM_024450261.1:c.4334A>T	XP_024306029.1:p.Asp1445Val
NM_001171.6:c.4298A>T MANE Select	NP_001162.5:p.Asp1433Val