Canonical Allele Identifier: CA7926368

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16198041A>G , CM000678.2:g.16198041A>G	GRCh38
NC_000016.9:g.16291898A>G , CM000678.1:g.16291898A>G	GRCh37
NC_000016.8:g.16199399A>G	NCBI36
NG_007558.2:g.30431T>C
NG_007558.3:g.30577T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574094.6:c.1318T>C	ENSP00000507301.1:p.Cys440Arg
ENST00000622290.5:c.1318T>C	ENSP00000483331.2:p.Cys440Arg
ENST00000205557.12:c.1318T>C MANE Select	ENSP00000205557.7:p.Cys440Arg
ENST00000205557.11:c.1318T>C	ENSP00000205557.7:p.Cys440Arg
ENST00000456970.6:c.1318T>C	ENSP00000405002.2:p.Cys440Arg
ENST00000574094.5:n.1414T>C
ENST00000622290.4:c.1318T>C	ENSP00000483331.1:p.Cys440Arg
NM_001171.5:c.1318T>C	NP_001162.4:p.Cys440Arg
XM_011522479.1:c.1318T>C	XP_011520781.1:p.Cys440Arg
XM_011522480.1:c.976T>C	XP_011520782.1:p.Cys326Arg
XM_011522481.1:c.976T>C	XP_011520783.1:p.Cys326Arg
XM_011522482.1:c.1318T>C	XP_011520784.1:p.Cys440Arg
XR_932836.1:n.1553T>C
XR_932837.1:n.1554T>C
XR_932838.1:n.1554T>C
NM_001351800.1:c.976T>C	NP_001338729.1:p.Cys326Arg
NR_147784.1:n.1355T>C
XM_011522479.2:c.1318T>C	XP_011520781.1:p.Cys440Arg
XM_011522481.3:c.976T>C	XP_011520783.1:p.Cys326Arg
XM_011522482.3:c.1318T>C	XP_011520784.1:p.Cys440Arg
XM_017023212.1:c.1318T>C	XP_016878701.1:p.Cys440Arg
XM_017023214.1:c.1318T>C	XP_016878703.1:p.Cys440Arg
XM_024450261.1:c.1354T>C	XP_024306029.1:p.Cys452Arg
XR_932836.2:n.1499T>C
XR_932837.3:n.1499T>C
XR_932838.3:n.1499T>C
NM_001171.6:c.1318T>C MANE Select	NP_001162.5:p.Cys440Arg