Canonical Allele Identifier: CA394883961

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16150720-G-A
• MyVariant Identifiers: chr16:g.16244577G>A (hg19) ; chr16:g.16150720G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150720G>A , CM000678.2:g.16150720G>A	GRCh38
NC_000016.9:g.16244577G>A , CM000678.1:g.16244577G>A	GRCh37
NC_000016.8:g.16152078G>A	NCBI36
NG_007558.2:g.77752C>T
NG_007558.3:g.77898C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*433C>T	ENSP00000483331.2:n.*433C>T
ENST00000205557.12:c.4261C>T MANE Select	ENSP00000205557.7:p.Gln1421Ter
ENST00000640696.1:c.1075C>T	ENSP00000492197.1:p.Gln359Ter
ENST00000205557.11:c.4261C>T	ENSP00000205557.7:p.Gln1421Ter
ENST00000456970.6:c.3886C>T	ENSP00000405002.2:n.3886C>T
ENST00000576204.5:n.1124C>T
ENST00000622290.4:c.*1470C>T	ENSP00000483331.1:n.*1470C>T
NM_001171.5:c.4261C>T	NP_001162.4:p.Gln1421Ter
XM_011522479.1:c.4228C>T	XP_011520781.1:p.Gln1410Ter
XM_011522480.1:c.3919C>T	XP_011520782.1:p.Gln1307Ter
XM_011522481.1:c.3919C>T	XP_011520783.1:p.Gln1307Ter
XR_933134.1:n.538+6430G>A
NM_001351800.1:c.3919C>T	NP_001338729.1:p.Gln1307Ter
NR_147784.1:n.3923C>T
XM_011522479.2:c.4228C>T	XP_011520781.1:p.Gln1410Ter
XM_011522481.3:c.3919C>T	XP_011520783.1:p.Gln1307Ter
XM_017023212.1:c.4093C>T	XP_016878701.1:p.Gln1365Ter
XM_024450261.1:c.4297C>T	XP_024306029.1:p.Gln1433Ter
NM_001171.6:c.4261C>T MANE Select	NP_001162.5:p.Gln1421Ter