Canonical Allele Identifier: CA394880439

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16256877A>C (hg19) ; chr16:g.16163020A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16163020A>C , CM000678.2:g.16163020A>C	GRCh38
NC_000016.9:g.16256877A>C , CM000678.1:g.16256877A>C	GRCh37
NC_000016.8:g.16164378A>C	NCBI36
NG_007558.2:g.65452T>G
NG_007558.3:g.65598T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3479T>G	ENSP00000483331.2:p.Ile1160Ser
ENST00000205557.12:c.3479T>G MANE Select	ENSP00000205557.7:p.Ile1160Ser
ENST00000640696.1:c.321-1456T>G	ENSP00000492197.1:n.321-1456T>G
ENST00000205557.11:c.3479T>G	ENSP00000205557.7:p.Ile1160Ser
ENST00000456970.6:c.3132-1456T>G	ENSP00000405002.2:n.3132-1456T>G
ENST00000622290.4:c.*688T>G	ENSP00000483331.1:n.*688T>G
NM_001171.5:c.3479T>G	NP_001162.4:p.Ile1160Ser
XM_011522479.1:c.3446T>G	XP_011520781.1:p.Ile1149Ser
XM_011522480.1:c.3137T>G	XP_011520782.1:p.Ile1046Ser
XM_011522481.1:c.3137T>G	XP_011520783.1:p.Ile1046Ser
XR_932836.1:n.3714T>G
XR_932837.1:n.3543-1456T>G
XR_932838.1:n.3543-1456T>G
XR_933133.1:n.407+177A>C
XR_933134.1:n.754+177A>C
NM_001351800.1:c.3137T>G	NP_001338729.1:p.Ile1046Ser
NR_147784.1:n.3169-1456T>G
XM_011522479.2:c.3446T>G	XP_011520781.1:p.Ile1149Ser
XM_011522481.3:c.3137T>G	XP_011520783.1:p.Ile1046Ser
XM_017023212.1:c.3311T>G	XP_016878701.1:p.Ile1104Ser
XM_017023214.1:c.3307-1456T>G	XP_016878703.1:n.3307-1456T>G
XM_024450261.1:c.3515T>G	XP_024306029.1:p.Ile1172Ser
XR_932836.2:n.3660T>G
XR_932837.3:n.3488-1456T>G
XR_932838.3:n.3488-1456T>G
NM_001171.6:c.3479T>G MANE Select	NP_001162.5:p.Ile1160Ser