Canonical Allele Identifier: CA2806038292

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16197985_16197986insGAGGGTGGGGGGGGGGGA , CM000678.2:g.16197985_16197986insGAGGGTGGGGGGGGGGGA	GRCh38
NC_000016.9:g.16291842_16291843insGAGGGTGGGGGGGGGGGA , CM000678.1:g.16291842_16291843insGAGGGTGGGGGGGGGGGA	GRCh37
NC_000016.8:g.16199343_16199344insGAGGGTGGGGGGGGGGGA	NCBI36
NG_007558.2:g.30492_30493insCCCCCCACCCTCTCCCCC
NG_007558.3:g.30638_30639insCCCCCCACCCTCTCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574094.6:c.1338+41_1338+42insCCCCCCACCCTCTCCCCC	ENSP00000507301.1:n.1338+41_1338+42insCCCCCCACCCTCTCCCCC
ENST00000622290.5:c.1338+41_1338+42insCCCCCCACCCTCTCCCCC	ENSP00000483331.2:n.1338+41_1338+42insCCCCCCACCCTCTCCCCC
ENST00000205557.12:c.1338+41_1338+42insCCCCCCACCCTCTCCCCC MANE Select	ENSP00000205557.7:n.1338+41_1338+42insCCCCCCACCCTCTCCCCC
ENST00000205557.11:c.1338+41_1338+42insCCCCCCACCCTCTCCCCC	ENSP00000205557.7:n.1338+41_1338+42insCCCCCCACCCTCTCCCCC
ENST00000456970.6:c.1338+41_1338+42insCCCCCCACCCTCTCCCCC	ENSP00000405002.2:n.1338+41_1338+42insCCCCCCACCCTCTCCCCC
ENST00000574094.5:n.1434+41_1434+42insCCCCCCACCCTCTCCCCC
ENST00000622290.4:c.1338+41_1338+42insCCCCCCACCCTCTCCCCC	ENSP00000483331.1:n.1338+41_1338+42insCCCCCCACCCTCTCCCCC
NM_001171.5:c.1338+41_1338+42insCCCCCCACCCTCTCCCCC	NP_001162.4:n.1338+41_1338+42insCCCCCCACCCTCTCCCCC
XM_011522479.1:c.1338+41_1338+42insCCCCCCACCCTCTCCCCC	XP_011520781.1:n.1338+41_1338+42insCCCCCCACCCTCTCCCCC
XM_011522480.1:c.996+41_996+42insCCCCCCACCCTCTCCCCC	XP_011520782.1:n.996+41_996+42insCCCCCCACCCTCTCCCCC
XM_011522481.1:c.996+41_996+42insCCCCCCACCCTCTCCCCC	XP_011520783.1:n.996+41_996+42insCCCCCCACCCTCTCCCCC
XM_011522482.1:c.1338+41_1338+42insCCCCCCACCCTCTCCCCC	XP_011520784.1:n.1338+41_1338+42insCCCCCCACCCTCTCCCCC
XR_932836.1:n.1573+41_1573+42insCCCCCCACCCTCTCCCCC
XR_932837.1:n.1574+41_1574+42insCCCCCCACCCTCTCCCCC
XR_932838.1:n.1574+41_1574+42insCCCCCCACCCTCTCCCCC
NM_001351800.1:c.996+41_996+42insCCCCCCACCCTCTCCCCC	NP_001338729.1:n.996+41_996+42insCCCCCCACCCTCTCCCCC
NR_147784.1:n.1375+41_1375+42insCCCCCCACCCTCTCCCCC
XM_011522479.2:c.1338+41_1338+42insCCCCCCACCCTCTCCCCC	XP_011520781.1:n.1338+41_1338+42insCCCCCCACCCTCTCCCCC
XM_011522481.3:c.996+41_996+42insCCCCCCACCCTCTCCCCC	XP_011520783.1:n.996+41_996+42insCCCCCCACCCTCTCCCCC
XM_011522482.3:c.1338+41_1338+42insCCCCCCACCCTCTCCCCC	XP_011520784.1:n.1338+41_1338+42insCCCCCCACCCTCTCCCCC
XM_017023212.1:c.1338+41_1338+42insCCCCCCACCCTCTCCCCC	XP_016878701.1:n.1338+41_1338+42insCCCCCCACCCTCTCCCCC
XM_017023214.1:c.1338+41_1338+42insCCCCCCACCCTCTCCCCC	XP_016878703.1:n.1338+41_1338+42insCCCCCCACCCTCTCCCCC
XM_024450261.1:c.1374+41_1374+42insCCCCCCACCCTCTCCCCC	XP_024306029.1:n.1374+41_1374+42insCCCCCCACCCTCTCCCCC
XR_932836.2:n.1519+41_1519+42insCCCCCCACCCTCTCCCCC
XR_932837.3:n.1519+41_1519+42insCCCCCCACCCTCTCCCCC
XR_932838.3:n.1519+41_1519+42insCCCCCCACCCTCTCCCCC
NM_001171.6:c.1338+41_1338+42insCCCCCCACCCTCTCCCCC MANE Select	NP_001162.5:n.1338+41_1338+42insCCCCCCACCCTCTCCCCC