Canonical Allele Identifier: CA394884059

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16244615T>A (hg19) ; chr16:g.16150758T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150758T>A , CM000678.2:g.16150758T>A	GRCh38
NC_000016.9:g.16244615T>A , CM000678.1:g.16244615T>A	GRCh37
NC_000016.8:g.16152116T>A	NCBI36
NG_007558.2:g.77714A>T
NG_007558.3:g.77860A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*395A>T	ENSP00000483331.2:n.*395A>T
ENST00000205557.12:c.4223A>T MANE Select	ENSP00000205557.7:p.Gln1408Leu
ENST00000640696.1:c.1037A>T	ENSP00000492197.1:p.Gln346Leu
ENST00000205557.11:c.4223A>T	ENSP00000205557.7:p.Gln1408Leu
ENST00000456970.6:c.3848A>T	ENSP00000405002.2:n.3848A>T
ENST00000576204.5:n.1086A>T
ENST00000622290.4:c.*1432A>T	ENSP00000483331.1:n.*1432A>T
NM_001171.5:c.4223A>T	NP_001162.4:p.Gln1408Leu
XM_011522479.1:c.4190A>T	XP_011520781.1:p.Gln1397Leu
XM_011522480.1:c.3881A>T	XP_011520782.1:p.Gln1294Leu
XM_011522481.1:c.3881A>T	XP_011520783.1:p.Gln1294Leu
XR_933134.1:n.538+6468T>A
NM_001351800.1:c.3881A>T	NP_001338729.1:p.Gln1294Leu
NR_147784.1:n.3885A>T
XM_011522479.2:c.4190A>T	XP_011520781.1:p.Gln1397Leu
XM_011522481.3:c.3881A>T	XP_011520783.1:p.Gln1294Leu
XM_017023212.1:c.4055A>T	XP_016878701.1:p.Gln1352Leu
XM_024450261.1:c.4259A>T	XP_024306029.1:p.Gln1420Leu
NM_001171.6:c.4223A>T MANE Select	NP_001162.5:p.Gln1408Leu