Canonical Allele Identifier: CA394876100

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16155004-C-A
• MyVariant Identifiers: chr16:g.16248861C>A (hg19) ; chr16:g.16155004C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16155004C>A , CM000678.2:g.16155004C>A	GRCh38
NC_000016.9:g.16248861C>A , CM000678.1:g.16248861C>A	GRCh37
NC_000016.8:g.16156362C>A	NCBI36
NG_007558.2:g.73468G>T
NG_007558.3:g.73614G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.773G>T
ENST00000622290.5:c.*82G>T	ENSP00000483331.2:n.*82G>T
ENST00000205557.12:c.3910G>T MANE Select	ENSP00000205557.7:p.Gly1304Trp
ENST00000640696.1:c.724G>T	ENSP00000492197.1:p.Gly242Trp
ENST00000205557.11:c.3910G>T	ENSP00000205557.7:p.Gly1304Trp
ENST00000456970.6:c.3535G>T	ENSP00000405002.2:n.3535G>T
ENST00000576204.5:n.773G>T
ENST00000622290.4:c.*1119G>T	ENSP00000483331.1:n.*1119G>T
NM_001171.5:c.3910G>T	NP_001162.4:p.Gly1304Trp
XM_011522479.1:c.3877G>T	XP_011520781.1:p.Gly1293Trp
XM_011522480.1:c.3568G>T	XP_011520782.1:p.Gly1190Trp
XM_011522481.1:c.3568G>T	XP_011520783.1:p.Gly1190Trp
XR_932836.1:n.4208G>T
XR_932837.1:n.3946G>T
XR_932838.1:n.4009G>T
XR_933134.1:n.539-4777C>A
NM_001351800.1:c.3568G>T	NP_001338729.1:p.Gly1190Trp
NR_147784.1:n.3572G>T
XM_011522479.2:c.3877G>T	XP_011520781.1:p.Gly1293Trp
XM_011522481.3:c.3568G>T	XP_011520783.1:p.Gly1190Trp
XM_017023212.1:c.3742G>T	XP_016878701.1:p.Gly1248Trp
XM_024450261.1:c.3946G>T	XP_024306029.1:p.Gly1316Trp
XR_932836.2:n.4154G>T
XR_932837.3:n.3891G>T
XR_932838.3:n.3954G>T
NM_001171.6:c.3910G>T MANE Select	NP_001162.5:p.Gly1304Trp