Canonical Allele Identifier: CA2533704815

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16197945-GGGAGGGGGAAGGAGGAGGGGGAGAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16197954_16197978del , CM000678.2:g.16197954_16197978del	GRCh38
NC_000016.9:g.16291811_16291835del , CM000678.1:g.16291811_16291835del	GRCh37
NC_000016.8:g.16199312_16199336del	NCBI36
NG_007558.2:g.30502_30526del
NG_007558.3:g.30648_30672del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574094.6:c.1338+51_1338+75del	ENSP00000507301.1:n.1338+51_1338+75del
ENST00000622290.5:c.1338+51_1338+75del	ENSP00000483331.2:n.1338+51_1338+75del
ENST00000205557.12:c.1338+51_1338+75del MANE Select	ENSP00000205557.7:n.1338+51_1338+75del
ENST00000205557.11:c.1338+51_1338+75del	ENSP00000205557.7:n.1338+51_1338+75del
ENST00000456970.6:c.1338+51_1338+75del	ENSP00000405002.2:n.1338+51_1338+75del
ENST00000574094.5:n.1434+51_1434+75del
ENST00000622290.4:c.1338+51_1338+75del	ENSP00000483331.1:n.1338+51_1338+75del
NM_001171.5:c.1338+51_1338+75del	NP_001162.4:n.1338+51_1338+75del
XM_011522479.1:c.1338+51_1338+75del	XP_011520781.1:n.1338+51_1338+75del
XM_011522480.1:c.996+51_996+75del	XP_011520782.1:n.996+51_996+75del
XM_011522481.1:c.996+51_996+75del	XP_011520783.1:n.996+51_996+75del
XM_011522482.1:c.1338+51_1338+75del	XP_011520784.1:n.1338+51_1338+75del
XR_932836.1:n.1573+51_1573+75del
XR_932837.1:n.1574+51_1574+75del
XR_932838.1:n.1574+51_1574+75del
NM_001351800.1:c.996+51_996+75del	NP_001338729.1:n.996+51_996+75del
NR_147784.1:n.1375+51_1375+75del
XM_011522479.2:c.1338+51_1338+75del	XP_011520781.1:n.1338+51_1338+75del
XM_011522481.3:c.996+51_996+75del	XP_011520783.1:n.996+51_996+75del
XM_011522482.3:c.1338+51_1338+75del	XP_011520784.1:n.1338+51_1338+75del
XM_017023212.1:c.1338+51_1338+75del	XP_016878701.1:n.1338+51_1338+75del
XM_017023214.1:c.1338+51_1338+75del	XP_016878703.1:n.1338+51_1338+75del
XM_024450261.1:c.1374+51_1374+75del	XP_024306029.1:n.1374+51_1374+75del
XR_932836.2:n.1519+51_1519+75del
XR_932837.3:n.1519+51_1519+75del
XR_932838.3:n.1519+51_1519+75del
NM_001171.6:c.1338+51_1338+75del MANE Select	NP_001162.5:n.1338+51_1338+75del