Canonical Allele Identifier: CA2806038441

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16198405_16198406del , CM000678.2:g.16198405_16198406del	GRCh38
NC_000016.9:g.16292262_16292263del , CM000678.1:g.16292262_16292263del	GRCh37
NC_000016.8:g.16199763_16199764del	NCBI36
NG_007558.2:g.30066_30067del
NG_007558.3:g.30212_30213del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574094.6:c.1177-224_1177-223del	ENSP00000507301.1:n.1177-224_1177-223del
ENST00000622290.5:c.1177-224_1177-223del	ENSP00000483331.2:n.1177-224_1177-223del
ENST00000205557.12:c.1177-224_1177-223del MANE Select	ENSP00000205557.7:n.1177-224_1177-223del
ENST00000205557.11:c.1177-224_1177-223del	ENSP00000205557.7:n.1177-224_1177-223del
ENST00000456970.6:c.1177-224_1177-223del	ENSP00000405002.2:n.1177-224_1177-223del
ENST00000574094.5:n.1273-224_1273-223del
ENST00000622290.4:c.1177-224_1177-223del	ENSP00000483331.1:n.1177-224_1177-223del
NM_001171.5:c.1177-224_1177-223del	NP_001162.4:n.1177-224_1177-223del
XM_011522479.1:c.1177-224_1177-223del	XP_011520781.1:n.1177-224_1177-223del
XM_011522480.1:c.835-224_835-223del	XP_011520782.1:n.835-224_835-223del
XM_011522481.1:c.835-224_835-223del	XP_011520783.1:n.835-224_835-223del
XM_011522482.1:c.1177-224_1177-223del	XP_011520784.1:n.1177-224_1177-223del
XR_932836.1:n.1412-224_1412-223del
XR_932837.1:n.1413-224_1413-223del
XR_932838.1:n.1413-224_1413-223del
NM_001351800.1:c.835-224_835-223del	NP_001338729.1:n.835-224_835-223del
NR_147784.1:n.1214-224_1214-223del
XM_011522479.2:c.1177-224_1177-223del	XP_011520781.1:n.1177-224_1177-223del
XM_011522481.3:c.835-224_835-223del	XP_011520783.1:n.835-224_835-223del
XM_011522482.3:c.1177-224_1177-223del	XP_011520784.1:n.1177-224_1177-223del
XM_017023212.1:c.1177-224_1177-223del	XP_016878701.1:n.1177-224_1177-223del
XM_017023214.1:c.1177-224_1177-223del	XP_016878703.1:n.1177-224_1177-223del
XM_024450261.1:c.1213-224_1213-223del	XP_024306029.1:n.1213-224_1213-223del
XR_932836.2:n.1358-224_1358-223del
XR_932837.3:n.1358-224_1358-223del
XR_932838.3:n.1358-224_1358-223del
NM_001171.6:c.1177-224_1177-223del MANE Select	NP_001162.5:n.1177-224_1177-223del