Canonical Allele Identifier: CA2806038417

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16198300_16198301insAGT , CM000678.2:g.16198300_16198301insAGT	GRCh38
NC_000016.9:g.16292157_16292158insAGT , CM000678.1:g.16292157_16292158insAGT	GRCh37
NC_000016.8:g.16199658_16199659insAGT	NCBI36
NG_007558.2:g.30171_30172insACT
NG_007558.3:g.30317_30318insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574094.6:c.1177-119_1177-118insACT	ENSP00000507301.1:n.1177-119_1177-118insACT
ENST00000622290.5:c.1177-119_1177-118insACT	ENSP00000483331.2:n.1177-119_1177-118insACT
ENST00000205557.12:c.1177-119_1177-118insACT MANE Select	ENSP00000205557.7:n.1177-119_1177-118insACT
ENST00000205557.11:c.1177-119_1177-118insACT	ENSP00000205557.7:n.1177-119_1177-118insACT
ENST00000456970.6:c.1177-119_1177-118insACT	ENSP00000405002.2:n.1177-119_1177-118insACT
ENST00000574094.5:n.1273-119_1273-118insACT
ENST00000622290.4:c.1177-119_1177-118insACT	ENSP00000483331.1:n.1177-119_1177-118insACT
NM_001171.5:c.1177-119_1177-118insACT	NP_001162.4:n.1177-119_1177-118insACT
XM_011522479.1:c.1177-119_1177-118insACT	XP_011520781.1:n.1177-119_1177-118insACT
XM_011522480.1:c.835-119_835-118insACT	XP_011520782.1:n.835-119_835-118insACT
XM_011522481.1:c.835-119_835-118insACT	XP_011520783.1:n.835-119_835-118insACT
XM_011522482.1:c.1177-119_1177-118insACT	XP_011520784.1:n.1177-119_1177-118insACT
XR_932836.1:n.1412-119_1412-118insACT
XR_932837.1:n.1413-119_1413-118insACT
XR_932838.1:n.1413-119_1413-118insACT
NM_001351800.1:c.835-119_835-118insACT	NP_001338729.1:n.835-119_835-118insACT
NR_147784.1:n.1214-119_1214-118insACT
XM_011522479.2:c.1177-119_1177-118insACT	XP_011520781.1:n.1177-119_1177-118insACT
XM_011522481.3:c.835-119_835-118insACT	XP_011520783.1:n.835-119_835-118insACT
XM_011522482.3:c.1177-119_1177-118insACT	XP_011520784.1:n.1177-119_1177-118insACT
XM_017023212.1:c.1177-119_1177-118insACT	XP_016878701.1:n.1177-119_1177-118insACT
XM_017023214.1:c.1177-119_1177-118insACT	XP_016878703.1:n.1177-119_1177-118insACT
XM_024450261.1:c.1213-119_1213-118insACT	XP_024306029.1:n.1213-119_1213-118insACT
XR_932836.2:n.1358-119_1358-118insACT
XR_932837.3:n.1358-119_1358-118insACT
XR_932838.3:n.1358-119_1358-118insACT
NM_001171.6:c.1177-119_1177-118insACT MANE Select	NP_001162.5:n.1177-119_1177-118insACT