Canonical Allele Identifier: CA493799712

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16248616G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154759G>A , CM000678.2:g.16154759G>A	GRCh38
NC_000016.9:g.16248616G>A , CM000678.1:g.16248616G>A	GRCh37
NC_000016.8:g.16156117G>A	NCBI36
NG_007558.2:g.73713C>T
NG_007558.3:g.73859C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.940C>T
ENST00000622290.5:c.*249C>T	ENSP00000483331.2:n.*249C>T
ENST00000205557.12:c.4077C>T MANE Select	ENSP00000205557.7:p.Asn1359=
ENST00000640696.1:c.891C>T	ENSP00000492197.1:p.Asn297=
ENST00000205557.11:c.4077C>T	ENSP00000205557.7:p.Asn1359=
ENST00000456970.6:c.3702C>T	ENSP00000405002.2:n.3702C>T
ENST00000576204.5:n.940C>T
ENST00000622290.4:c.*1286C>T	ENSP00000483331.1:n.*1286C>T
NM_001171.5:c.4077C>T	NP_001162.4:p.Asn1359=
XM_011522479.1:c.4044C>T	XP_011520781.1:p.Asn1348=
XM_011522480.1:c.3735C>T	XP_011520782.1:p.Asn1245=
XM_011522481.1:c.3735C>T	XP_011520783.1:p.Asn1245=
XR_933134.1:n.539-5022G>A
NM_001351800.1:c.3735C>T	NP_001338729.1:p.Asn1245=
NR_147784.1:n.3739C>T
XM_011522479.2:c.4044C>T	XP_011520781.1:p.Asn1348=
XM_011522481.3:c.3735C>T	XP_011520783.1:p.Asn1245=
XM_017023212.1:c.3909C>T	XP_016878701.1:p.Asn1303=
XM_024450261.1:c.4113C>T	XP_024306029.1:p.Asn1371=
NM_001171.6:c.4077C>T MANE Select	NP_001162.5:p.Asn1359=