Canonical Allele Identifier: CA975113318

Gene: ABCC6

Linked Data

• gnomAD v3: 16-16197973-A-AGGGGGGGGGGAGGGGG
• gnomAD v4: 16-16197973-A-AGGGGGGGGGGAGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16197978_16197979insGGGGGAGGGGGGGGGG , CM000678.2:g.16197978_16197979insGGGGGAGGGGGGGGGG	GRCh38
NC_000016.9:g.16291835_16291836insGGGGGAGGGGGGGGGG , CM000678.1:g.16291835_16291836insGGGGGAGGGGGGGGGG	GRCh37
NC_000016.8:g.16199336_16199337insGGGGGAGGGGGGGGGG	NCBI36
NG_007558.2:g.30498_30499insCCCCCTCCCCCCCCCC
NG_007558.3:g.30644_30645insCCCCCTCCCCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574094.6:c.1338+47_1338+48insCCCCCTCCCCCCCCCC	ENSP00000507301.1:n.1338+47_1338+48insCCCCCTCCCCCCCCCC
ENST00000622290.5:c.1338+47_1338+48insCCCCCTCCCCCCCCCC	ENSP00000483331.2:n.1338+47_1338+48insCCCCCTCCCCCCCCCC
ENST00000205557.12:c.1338+47_1338+48insCCCCCTCCCCCCCCCC MANE Select	ENSP00000205557.7:n.1338+47_1338+48insCCCCCTCCCCCCCCCC
ENST00000205557.11:c.1338+47_1338+48insCCCCCTCCCCCCCCCC	ENSP00000205557.7:n.1338+47_1338+48insCCCCCTCCCCCCCCCC
ENST00000456970.6:c.1338+47_1338+48insCCCCCTCCCCCCCCCC	ENSP00000405002.2:n.1338+47_1338+48insCCCCCTCCCCCCCCCC
ENST00000574094.5:n.1434+47_1434+48insCCCCCTCCCCCCCCCC
ENST00000622290.4:c.1338+47_1338+48insCCCCCTCCCCCCCCCC	ENSP00000483331.1:n.1338+47_1338+48insCCCCCTCCCCCCCCCC
NM_001171.5:c.1338+47_1338+48insCCCCCTCCCCCCCCCC	NP_001162.4:n.1338+47_1338+48insCCCCCTCCCCCCCCCC
XM_011522479.1:c.1338+47_1338+48insCCCCCTCCCCCCCCCC	XP_011520781.1:n.1338+47_1338+48insCCCCCTCCCCCCCCCC
XM_011522480.1:c.996+47_996+48insCCCCCTCCCCCCCCCC	XP_011520782.1:n.996+47_996+48insCCCCCTCCCCCCCCCC
XM_011522481.1:c.996+47_996+48insCCCCCTCCCCCCCCCC	XP_011520783.1:n.996+47_996+48insCCCCCTCCCCCCCCCC
XM_011522482.1:c.1338+47_1338+48insCCCCCTCCCCCCCCCC	XP_011520784.1:n.1338+47_1338+48insCCCCCTCCCCCCCCCC
XR_932836.1:n.1573+47_1573+48insCCCCCTCCCCCCCCCC
XR_932837.1:n.1574+47_1574+48insCCCCCTCCCCCCCCCC
XR_932838.1:n.1574+47_1574+48insCCCCCTCCCCCCCCCC
NM_001351800.1:c.996+47_996+48insCCCCCTCCCCCCCCCC	NP_001338729.1:n.996+47_996+48insCCCCCTCCCCCCCCCC
NR_147784.1:n.1375+47_1375+48insCCCCCTCCCCCCCCCC
XM_011522479.2:c.1338+47_1338+48insCCCCCTCCCCCCCCCC	XP_011520781.1:n.1338+47_1338+48insCCCCCTCCCCCCCCCC
XM_011522481.3:c.996+47_996+48insCCCCCTCCCCCCCCCC	XP_011520783.1:n.996+47_996+48insCCCCCTCCCCCCCCCC
XM_011522482.3:c.1338+47_1338+48insCCCCCTCCCCCCCCCC	XP_011520784.1:n.1338+47_1338+48insCCCCCTCCCCCCCCCC
XM_017023212.1:c.1338+47_1338+48insCCCCCTCCCCCCCCCC	XP_016878701.1:n.1338+47_1338+48insCCCCCTCCCCCCCCCC
XM_017023214.1:c.1338+47_1338+48insCCCCCTCCCCCCCCCC	XP_016878703.1:n.1338+47_1338+48insCCCCCTCCCCCCCCCC
XM_024450261.1:c.1374+47_1374+48insCCCCCTCCCCCCCCCC	XP_024306029.1:n.1374+47_1374+48insCCCCCTCCCCCCCCCC
XR_932836.2:n.1519+47_1519+48insCCCCCTCCCCCCCCCC
XR_932837.3:n.1519+47_1519+48insCCCCCTCCCCCCCCCC
XR_932838.3:n.1519+47_1519+48insCCCCCTCCCCCCCCCC
NM_001171.6:c.1338+47_1338+48insCCCCCTCCCCCCCCCC MANE Select	NP_001162.5:n.1338+47_1338+48insCCCCCTCCCCCCCCCC