Canonical Allele Identifier: CA394883960

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16244576T>G (hg19) ; chr16:g.16150719T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150719T>G , CM000678.2:g.16150719T>G	GRCh38
NC_000016.9:g.16244576T>G , CM000678.1:g.16244576T>G	GRCh37
NC_000016.8:g.16152077T>G	NCBI36
NG_007558.2:g.77753A>C
NG_007558.3:g.77899A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*434A>C	ENSP00000483331.2:n.*434A>C
ENST00000205557.12:c.4262A>C MANE Select	ENSP00000205557.7:p.Gln1421Pro
ENST00000640696.1:c.1076A>C	ENSP00000492197.1:p.Gln359Pro
ENST00000205557.11:c.4262A>C	ENSP00000205557.7:p.Gln1421Pro
ENST00000456970.6:c.3887A>C	ENSP00000405002.2:n.3887A>C
ENST00000576204.5:n.1125A>C
ENST00000622290.4:c.*1471A>C	ENSP00000483331.1:n.*1471A>C
NM_001171.5:c.4262A>C	NP_001162.4:p.Gln1421Pro
XM_011522479.1:c.4229A>C	XP_011520781.1:p.Gln1410Pro
XM_011522480.1:c.3920A>C	XP_011520782.1:p.Gln1307Pro
XM_011522481.1:c.3920A>C	XP_011520783.1:p.Gln1307Pro
XR_933134.1:n.538+6429T>G
NM_001351800.1:c.3920A>C	NP_001338729.1:p.Gln1307Pro
NR_147784.1:n.3924A>C
XM_011522479.2:c.4229A>C	XP_011520781.1:p.Gln1410Pro
XM_011522481.3:c.3920A>C	XP_011520783.1:p.Gln1307Pro
XM_017023212.1:c.4094A>C	XP_016878701.1:p.Gln1365Pro
XM_024450261.1:c.4298A>C	XP_024306029.1:p.Gln1433Pro
NM_001171.6:c.4262A>C MANE Select	NP_001162.5:p.Gln1421Pro