Canonical Allele Identifier: CA2806038366

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16198236_16198237insAG , CM000678.2:g.16198236_16198237insAG	GRCh38
NC_000016.9:g.16292093_16292094insAG , CM000678.1:g.16292093_16292094insAG	GRCh37
NC_000016.8:g.16199594_16199595insAG	NCBI36
NG_007558.2:g.30235_30236insCT
NG_007558.3:g.30381_30382insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574094.6:c.1177-55_1177-54insCT	ENSP00000507301.1:n.1177-55_1177-54insCT
ENST00000622290.5:c.1177-55_1177-54insCT	ENSP00000483331.2:n.1177-55_1177-54insCT
ENST00000205557.12:c.1177-55_1177-54insCT MANE Select	ENSP00000205557.7:n.1177-55_1177-54insCT
ENST00000205557.11:c.1177-55_1177-54insCT	ENSP00000205557.7:n.1177-55_1177-54insCT
ENST00000456970.6:c.1177-55_1177-54insCT	ENSP00000405002.2:n.1177-55_1177-54insCT
ENST00000574094.5:n.1273-55_1273-54insCT
ENST00000622290.4:c.1177-55_1177-54insCT	ENSP00000483331.1:n.1177-55_1177-54insCT
NM_001171.5:c.1177-55_1177-54insCT	NP_001162.4:n.1177-55_1177-54insCT
XM_011522479.1:c.1177-55_1177-54insCT	XP_011520781.1:n.1177-55_1177-54insCT
XM_011522480.1:c.835-55_835-54insCT	XP_011520782.1:n.835-55_835-54insCT
XM_011522481.1:c.835-55_835-54insCT	XP_011520783.1:n.835-55_835-54insCT
XM_011522482.1:c.1177-55_1177-54insCT	XP_011520784.1:n.1177-55_1177-54insCT
XR_932836.1:n.1412-55_1412-54insCT
XR_932837.1:n.1413-55_1413-54insCT
XR_932838.1:n.1413-55_1413-54insCT
NM_001351800.1:c.835-55_835-54insCT	NP_001338729.1:n.835-55_835-54insCT
NR_147784.1:n.1214-55_1214-54insCT
XM_011522479.2:c.1177-55_1177-54insCT	XP_011520781.1:n.1177-55_1177-54insCT
XM_011522481.3:c.835-55_835-54insCT	XP_011520783.1:n.835-55_835-54insCT
XM_011522482.3:c.1177-55_1177-54insCT	XP_011520784.1:n.1177-55_1177-54insCT
XM_017023212.1:c.1177-55_1177-54insCT	XP_016878701.1:n.1177-55_1177-54insCT
XM_017023214.1:c.1177-55_1177-54insCT	XP_016878703.1:n.1177-55_1177-54insCT
XM_024450261.1:c.1213-55_1213-54insCT	XP_024306029.1:n.1213-55_1213-54insCT
XR_932836.2:n.1358-55_1358-54insCT
XR_932837.3:n.1358-55_1358-54insCT
XR_932838.3:n.1358-55_1358-54insCT
NM_001171.6:c.1177-55_1177-54insCT MANE Select	NP_001162.5:n.1177-55_1177-54insCT