Canonical Allele Identifier: CA2806038363

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16198233_16198234insA , CM000678.2:g.16198233_16198234insA	GRCh38
NC_000016.9:g.16292090_16292091insA , CM000678.1:g.16292090_16292091insA	GRCh37
NC_000016.8:g.16199591_16199592insA	NCBI36
NG_007558.2:g.30238_30239insT
NG_007558.3:g.30384_30385insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574094.6:c.1177-52_1177-51insT	ENSP00000507301.1:n.1177-52_1177-51insT
ENST00000622290.5:c.1177-52_1177-51insT	ENSP00000483331.2:n.1177-52_1177-51insT
ENST00000205557.12:c.1177-52_1177-51insT MANE Select	ENSP00000205557.7:n.1177-52_1177-51insT
ENST00000205557.11:c.1177-52_1177-51insT	ENSP00000205557.7:n.1177-52_1177-51insT
ENST00000456970.6:c.1177-52_1177-51insT	ENSP00000405002.2:n.1177-52_1177-51insT
ENST00000574094.5:n.1273-52_1273-51insT
ENST00000622290.4:c.1177-52_1177-51insT	ENSP00000483331.1:n.1177-52_1177-51insT
NM_001171.5:c.1177-52_1177-51insT	NP_001162.4:n.1177-52_1177-51insT
XM_011522479.1:c.1177-52_1177-51insT	XP_011520781.1:n.1177-52_1177-51insT
XM_011522480.1:c.835-52_835-51insT	XP_011520782.1:n.835-52_835-51insT
XM_011522481.1:c.835-52_835-51insT	XP_011520783.1:n.835-52_835-51insT
XM_011522482.1:c.1177-52_1177-51insT	XP_011520784.1:n.1177-52_1177-51insT
XR_932836.1:n.1412-52_1412-51insT
XR_932837.1:n.1413-52_1413-51insT
XR_932838.1:n.1413-52_1413-51insT
NM_001351800.1:c.835-52_835-51insT	NP_001338729.1:n.835-52_835-51insT
NR_147784.1:n.1214-52_1214-51insT
XM_011522479.2:c.1177-52_1177-51insT	XP_011520781.1:n.1177-52_1177-51insT
XM_011522481.3:c.835-52_835-51insT	XP_011520783.1:n.835-52_835-51insT
XM_011522482.3:c.1177-52_1177-51insT	XP_011520784.1:n.1177-52_1177-51insT
XM_017023212.1:c.1177-52_1177-51insT	XP_016878701.1:n.1177-52_1177-51insT
XM_017023214.1:c.1177-52_1177-51insT	XP_016878703.1:n.1177-52_1177-51insT
XM_024450261.1:c.1213-52_1213-51insT	XP_024306029.1:n.1213-52_1213-51insT
XR_932836.2:n.1358-52_1358-51insT
XR_932837.3:n.1358-52_1358-51insT
XR_932838.3:n.1358-52_1358-51insT
NM_001171.6:c.1177-52_1177-51insT MANE Select	NP_001162.5:n.1177-52_1177-51insT