Canonical Allele Identifier: CA394882801

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16259536T>A (hg19) ; chr16:g.16165679T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16165679T>A , CM000678.2:g.16165679T>A	GRCh38
NC_000016.9:g.16259536T>A , CM000678.1:g.16259536T>A	GRCh37
NC_000016.8:g.16167037T>A	NCBI36
NG_007558.2:g.62793A>T
NG_007558.3:g.62939A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3250A>T	ENSP00000483331.2:p.Thr1084Ser
ENST00000205557.12:c.3250A>T MANE Select	ENSP00000205557.7:p.Thr1084Ser
ENST00000640696.1:c.265A>T	ENSP00000492197.1:p.Thr89Ser
ENST00000205557.11:c.3250A>T	ENSP00000205557.7:p.Thr1084Ser
ENST00000456970.6:c.3075A>T	ENSP00000405002.2:n.3075A>T
ENST00000622290.4:c.*459A>T	ENSP00000483331.1:n.*459A>T
NM_001171.5:c.3250A>T	NP_001162.4:p.Thr1084Ser
XM_011522479.1:c.3217A>T	XP_011520781.1:p.Thr1073Ser
XM_011522480.1:c.2908A>T	XP_011520782.1:p.Thr970Ser
XM_011522481.1:c.2908A>T	XP_011520783.1:p.Thr970Ser
XR_932836.1:n.3485A>T
XR_932837.1:n.3486A>T
XR_932838.1:n.3486A>T
NM_001351800.1:c.2908A>T	NP_001338729.1:p.Thr970Ser
NR_147784.1:n.3112A>T
XM_011522479.2:c.3217A>T	XP_011520781.1:p.Thr1073Ser
XM_011522481.3:c.2908A>T	XP_011520783.1:p.Thr970Ser
XM_017023212.1:c.3082A>T	XP_016878701.1:p.Thr1028Ser
XM_017023214.1:c.3250A>T	XP_016878703.1:p.Thr1084Ser
XM_024450261.1:c.3286A>T	XP_024306029.1:p.Thr1096Ser
XR_932836.2:n.3431A>T
XR_932837.3:n.3431A>T
XR_932838.3:n.3431A>T
NM_001171.6:c.3250A>T MANE Select	NP_001162.5:p.Thr1084Ser