Canonical Allele Identifier: CA394882821

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16259539C>T (hg19) ; chr16:g.16165682C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16165682C>T , CM000678.2:g.16165682C>T	GRCh38
NC_000016.9:g.16259539C>T , CM000678.1:g.16259539C>T	GRCh37
NC_000016.8:g.16167040C>T	NCBI36
NG_007558.2:g.62790G>A
NG_007558.3:g.62936G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3247G>A	ENSP00000483331.2:p.Ala1083Thr
ENST00000205557.12:c.3247G>A MANE Select	ENSP00000205557.7:p.Ala1083Thr
ENST00000640696.1:c.262G>A	ENSP00000492197.1:p.Ala88Thr
ENST00000205557.11:c.3247G>A	ENSP00000205557.7:p.Ala1083Thr
ENST00000456970.6:c.3072G>A	ENSP00000405002.2:n.3072G>A
ENST00000622290.4:c.*456G>A	ENSP00000483331.1:n.*456G>A
NM_001171.5:c.3247G>A	NP_001162.4:p.Ala1083Thr
XM_011522479.1:c.3214G>A	XP_011520781.1:p.Ala1072Thr
XM_011522480.1:c.2905G>A	XP_011520782.1:p.Ala969Thr
XM_011522481.1:c.2905G>A	XP_011520783.1:p.Ala969Thr
XR_932836.1:n.3482G>A
XR_932837.1:n.3483G>A
XR_932838.1:n.3483G>A
NM_001351800.1:c.2905G>A	NP_001338729.1:p.Ala969Thr
NR_147784.1:n.3109G>A
XM_011522479.2:c.3214G>A	XP_011520781.1:p.Ala1072Thr
XM_011522481.3:c.2905G>A	XP_011520783.1:p.Ala969Thr
XM_017023212.1:c.3079G>A	XP_016878701.1:p.Ala1027Thr
XM_017023214.1:c.3247G>A	XP_016878703.1:p.Ala1083Thr
XM_024450261.1:c.3283G>A	XP_024306029.1:p.Ala1095Thr
XR_932836.2:n.3428G>A
XR_932837.3:n.3428G>A
XR_932838.3:n.3428G>A
NM_001171.6:c.3247G>A MANE Select	NP_001162.5:p.Ala1083Thr