Canonical Allele Identifier: CA2806037117

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159683_16159684insACA , CM000678.2:g.16159683_16159684insACA	GRCh38
NC_000016.9:g.16253540_16253541insACA , CM000678.1:g.16253540_16253541insACA	GRCh37
NC_000016.8:g.16161041_16161042insACA	NCBI36
NG_007558.2:g.68788_68789insTGT
NG_007558.3:g.68934_68935insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3634-101_3634-100insTGT	ENSP00000483331.2:n.3634-101_3634-100insTGT
ENST00000205557.12:c.3634-101_3634-100insTGT MANE Select	ENSP00000205557.7:n.3634-101_3634-100insTGT
ENST00000640696.1:c.448-101_448-100insTGT	ENSP00000492197.1:n.448-101_448-100insTGT
ENST00000205557.11:c.3634-101_3634-100insTGT	ENSP00000205557.7:n.3634-101_3634-100insTGT
ENST00000456970.6:c.3259-101_3259-100insTGT	ENSP00000405002.2:n.3259-101_3259-100insTGT
ENST00000622290.4:c.*843-101_*843-100insTGT	ENSP00000483331.1:n.*843-101_*843-100insTGT
NM_001171.5:c.3634-101_3634-100insTGT	NP_001162.4:n.3634-101_3634-100insTGT
XM_011522479.1:c.3601-101_3601-100insTGT	XP_011520781.1:n.3601-101_3601-100insTGT
XM_011522480.1:c.3292-101_3292-100insTGT	XP_011520782.1:n.3292-101_3292-100insTGT
XM_011522481.1:c.3292-101_3292-100insTGT	XP_011520783.1:n.3292-101_3292-100insTGT
XR_932836.1:n.3869-101_3869-100insTGT
XR_932837.1:n.3670-101_3670-100insTGT
XR_932838.1:n.3670-101_3670-100insTGT
XR_933133.1:n.94_95insACA
XR_933134.1:n.539-98_539-97insACA
NM_001351800.1:c.3292-101_3292-100insTGT	NP_001338729.1:n.3292-101_3292-100insTGT
NR_147784.1:n.3296-101_3296-100insTGT
XM_011522479.2:c.3601-101_3601-100insTGT	XP_011520781.1:n.3601-101_3601-100insTGT
XM_011522481.3:c.3292-101_3292-100insTGT	XP_011520783.1:n.3292-101_3292-100insTGT
XM_017023212.1:c.3466-101_3466-100insTGT	XP_016878701.1:n.3466-101_3466-100insTGT
XM_024450261.1:c.3670-101_3670-100insTGT	XP_024306029.1:n.3670-101_3670-100insTGT
XR_932836.2:n.3815-101_3815-100insTGT
XR_932837.3:n.3615-101_3615-100insTGT
XR_932838.3:n.3615-101_3615-100insTGT
NM_001171.6:c.3634-101_3634-100insTGT MANE Select	NP_001162.5:n.3634-101_3634-100insTGT